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Adams-Oliver syndrome

Disease Summary
Associated Targets (7)
Tbio

5

Tchem

2


GARD Rare
Mondo Description Adams-Oliver Syndrome (AOS) is a rare disorder characterized by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects.
Disease Ontology Description A syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs.
Mondo Term and Equivalent IDs
MONDO:0007034:  Adams-Oliver syndrome
GARD:0005739: 
MESH:C538225: 
OMIMPS:100300: 
Orphanet:974: 
SCTID:34748004: 
UMLS:C0265268: