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Echinobase
Summary Literature (0)
DOID:0050471 - Carney complex

Disease Ontology Definition:A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.

Synonyms: Carney complex variant, Carney Complex, Type 1, Carney Complex, Type 2, Carney Syndrome, LAMB Syndrome, NAME Syndrome

Echinobase Genes :


MIM:
MIM:160980 - carney complex, type 1; cnc1
MIM:608837 - carney complex variant

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

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