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ONTOLOGY REPORT - ANNOTATIONS


Term:Geleophysic Dysplasia 3
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Accession:DOID:9009065 term browser browse the term
Definition:GPHYSD3 is caused by heterozygous mutation in the LTBP3 gene (602090) on chromosome 11q13. (OMIM)
Synonyms:exact_synonym: GPHYSD3
 primary_id: OMIM:617809
For additional species annotation, visit the Alliance of Genome Resources.


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Geleophysic Dysplasia 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ltbp3 latent transforming growth factor beta binding protein 3 JBrowse link 1 221,099,155 221,116,096 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    Pathological Conditions, Signs and Symptoms 8030
      Pathologic Processes 5078
        Growth Disorders 246
          Geleophysic Dysplasia 3
            Geleophysic Dysplasia 3 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      Skin and Connective Tissue Diseases 4211
        connective tissue disease 2763
          bone disease 2215
            bone development disease 983
              osteochondrodysplasia 408
                acromicric dysplasia 5
                  Geleophysic Dysplasia 3
                    Geleophysic Dysplasia 3 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.