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DOID:14759 - autosomal recessive type IV Ehlers-Danlos syndrome
Disease Ontology Definition:An Ehlers-Danlos syndrome 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.
Synonyms: Ehlers-Danlos syndrome, recessive type 4, Ehlers-Danlos syndrome, recessive type 4 (disorder),
Xenbase Genes :
MONDO:0002014 - autosomal recessive Ehlers-Danlos syndrome, vascular type |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee