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GENE - TERM ANNOTATION REPORT

60 Annotations Found.

An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:13436883 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21405769 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906113 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906142 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12838685 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906150 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12834196 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574283 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574284 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906161 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906147 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906154 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574754 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24135949


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574281 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906143 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8555155 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24135949, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906137 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:25512148, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906126 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906123 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574755 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24135949, PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906111 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8555154 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24135949, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:11633188 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906117 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574282 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12906132 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273, PMID:26387786


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574280 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Familial pulmonary capillary hemangiomatosis
  • Original References(s): PMID:24292273


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12847264 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21405432 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21406228 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21405728 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21406020 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21405448 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12838789 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21406227 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21406023 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12834595 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12847476 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12837456 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12844607 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12833678 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12843964 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:12840901 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24033266


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404824 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404817 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404807 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404823 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404803 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404815 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404810 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404805 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404820 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404804 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404812 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404809 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404822 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:8574279 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:24135949, PMID:24292273, PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404813 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


  • An association has been curated linking EIF2AK4 and Pulmonary Venoocclusive Disease 2 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:21404826 (Homo sapiens)
  • 1 CRRD objects have been annotated to Pulmonary Venoocclusive Disease 2  (DOID:9007143)
  • 7 papers in CRRD have been used to annotate EIF2AK4
  • Curation Notes: ClinVar Annotator: match by term: Pulmonary venoocclusive disease 2, autosomal recessive
  • Original References(s): PMID:32581362


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