Summary Literature (0)

DOID:0060227 - Adams-Oliver syndrome

Disease Ontology Definition:A syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs.

Synonyms: Adams Oliver syndrome

Xenbase Genes : notch1, dll4, rbpj, dock6, eogt, arhgap31

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007034 - Adams-Oliver syndrome

MIM:

MIM:100300 - ADAMS-OLIVER SYNDROME 1; AOS1

MIM:614219 - ADAMS-OLIVER SYNDROME 2; AOS2

MIM:614814 - ADAMS-OLIVER SYNDROME 3; AOS3

MIM:615297 - ADAMS-OLIVER SYNDROME 4; AOS4

MIM:616028 - ADAMS-OLIVER SYNDROME 5; AOS5

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee