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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

In OMIM:
OMIM:100300 - ADAMS-OLIVER SYNDROME 1; AOS1
OMIM:614219 - ADAMS-OLIVER SYNDROME 2; AOS2
OMIM:614814 - ADAMS-OLIVER SYNDROME 3; AOS3
OMIM:615297 - ADAMS-OLIVER SYNDROME 4; AOS4
OMIM:616028 - ADAMS-OLIVER SYNDROME 5; AOS5

In Mondo Disease Ontology:
MONDO:0007034 - Adams-Oliver syndrome

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): syndrome (is_a)