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Echinobase
Summary Literature (0)
DOID:0060330 - Rapp-Hodgkin syndrome

Disease Ontology Definition:An autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate.

Synonyms: anhidrotic ectodermal dysplasia with cleft lip/palate,

Echinobase Genes :


OMIM:
MIM:129400 - rapp-hodgkin syndrome; rhs

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a)