Adams-Oliver syndrome

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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

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: rbpj, eogt, rbpj

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: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

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

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

Parent(s): syndrome (is_a)