autosomal recessive type IV Ehlers-Danlos syndrome (DOID:14759)
Alliance: disease page
Synonyms: Ehlers-Danlos syndrome, recessive type 4
Alt IDs: UMLS_CUI:C0268340
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.