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ONTOLOGY REPORT - ANNOTATIONS


Term:Geleophysic Dysplasia 2
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Accession:DOID:9005971 term browser browse the term
Definition:GPHYSD2 is an autosomal dominant form of the disorder caused by heterozygous mutation in exon 41 or 42 of the FBN1 gene on chromosome 15q21.1. (OMIM)
Synonyms:exact_synonym: GPHYSD2
 primary_id: OMIM:614185
 alt_id: RDO:9000311
For additional species annotation, visit the Alliance of Genome Resources.


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Geleophysic Dysplasia 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fbn1 fibrillin 1 JBrowse link NW_004936471 10,747,030 10,969,223 RGD:7240710
RGD:9068941

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Path 1
Term Annotations click to browse term
  disease 11368
    Pathological Conditions, Signs and Symptoms 6552
      Pathologic Processes 4316
        Growth Disorders 218
          Geleophysic Dysplasia 3
            Geleophysic Dysplasia 2 1
Path 2
Term Annotations click to browse term
  disease 11368
    disease of anatomical entity 11036
      Skin and Connective Tissue Diseases 3465
        connective tissue disease 2248
          bone disease 1760
            bone development disease 960
              osteochondrodysplasia 396
                acromicric dysplasia 5
                  Geleophysic Dysplasia 3
                    Geleophysic Dysplasia 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.