Search Ontology:
Human Disease
vascular type Ehlers-Danlos syndrome
- Term ID
- DOID:14756
- Synonyms
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- autosomal dominant type IV Ehlers-Danlos syndrome
- Definition
- An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the COL3A1 gene on chromosome 2q32 and that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits. https://pubmed.ncbi.nlm.nih.gov/21637106/
- References
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- GARD:2082
- MIM:130050
- NCI:C125699
- ORDO:286
- Ontology
- Human Disease ( DOID:14756 )
- is a type of
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Genes Involved
Zebrafish Models