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GENE - TERM ANNOTATION REPORT

115 Annotations Found.

An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Gallione CJ, etal., J Med Genet. 2006 Oct;43(10):793-7. Epub 2006 Apr 13.
  • 4 additional annotations were made from Gallione CJ, etal., J Med Genet. 2006 Oct;43(10):793-7. Epub 2006 Apr 13.
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: DNA:missense,frameshift, nonsense mutations:exons:

  • This annotation was curated on 2018-04-07 09:00:21.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645153 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:43.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11635157 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617611 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:31.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651277 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:43.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618497 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:44.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613475 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:00.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628370 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:56.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665481 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:28.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8567602 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:16436638, PMID:22875147, PMID:25741868, PMID:26467025, PMID:27613157, PMID:28492532

  • This annotation was curated on 2019-12-03 05:56:57.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11345765 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-12-03 06:01:15.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692955 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868, PMID:25980754, PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-12-03 06:00:34.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627040 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:32.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626583 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:20.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615463 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645143 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:42.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649200 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:40.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653565 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:17.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612915 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-12-03 06:00:07.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650647 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:38.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649920 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:33.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627100 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:20.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646513 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:58.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11629035 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:53.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627572 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:33.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645142 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:42.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644860 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:13.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654014 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:08.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11634827 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:16.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650595 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:40.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626408 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645867 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651211 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:08.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617504 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:15.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650327 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:58.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612704 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626271 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:14.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626908 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:46.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646449 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:20.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652800 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:33.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649555 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:36.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11635172 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:24.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647221 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:45.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627933 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11644574 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:29.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653723 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:21.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649639 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:35.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617012 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:38.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626379 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:44.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692957 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-12-03 06:00:34.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628994 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:49.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615768 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:08.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11617023 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:39.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628687 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:03.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615467 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627868 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:20.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11651781 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:43.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627979 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:49.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648621 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:59.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645055 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:12.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626821 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:17.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627305 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:52.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648671 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:24.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615141 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:08.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614996 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:57.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652849 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:09.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628069 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653513 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:46.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626991 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:05.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11614062 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:32.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627154 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:45.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11649695 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:26.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648551 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:34.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11612714 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:01:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647982 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:57.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628074 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615012 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:58.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628550 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:18.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11646295 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:57:20.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618263 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:44.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626910 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:46.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645973 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:13.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647803 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:19.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615331 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:57.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626982 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:40.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11665446 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:14.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626968 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:39.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626328 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:16.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11626653 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:39.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628395 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:21.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11653107 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:48.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627484 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:56:14.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645933 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:54.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647404 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:23.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627981 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:50.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11650129 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:09.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627864 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:19.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11615365 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:44.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627954 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:55:24.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647835 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:47.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11618524 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:50.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613899 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:54.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11648079 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:28.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11645642 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:44.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11613582 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11652007 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 06:00:11.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11627633 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:58:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11647318 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:22.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628302 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:33.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11654163 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome

  • This annotation was curated on 2019-12-03 05:59:23.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8688731 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:10790223, PMID:15288293, PMID:21835029, PMID:24465802, PMID:25695693, PMID:25741868, PMID:26467025, PMID:28492532

  • This annotation was curated on 2019-12-03 05:59:06.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9834758 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868, PMID:28135145, PMID:28492532

  • This annotation was curated on 2019-12-03 05:58:13.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8604907 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:21835029, PMID:22703879, PMID:23399955, PMID:25148578, PMID:25186627, PMID:25318351, PMID:25637381, PMID:25741868, PMID:25980754, PMID:26467025, PMID:27153395, PMID:28492532

  • This annotation was curated on 2019-12-03 06:00:58.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11628071 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25741868, PMID:28492532

  • This annotation was curated on 2019-12-03 05:57:10.0 by CRRD . For more information contact us

    An association has been curated linking SMAD4 and hereditary hemorrhagic telangiectasia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8658840 (Homo sapiens)
  • 7 CRRD objects have been annotated to hereditary hemorrhagic telangiectasia  (DOID:1270)
  • 57 papers in CRRD have been used to annotate SMAD4
  • Curation Notes: ClinVar Annotator: match by term: Osler hemorrhagic telangiectasia syndrome
  • Original References(s): PMID:25186627, PMID:25741868, PMID:25980754, PMID:26467025, PMID:27146957, PMID:28492532, PMID:28726808, PMID:28873162

  • This annotation was curated on 2019-12-03 05:56:38.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.