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DOID:0050471 - Carney complex
Disease Ontology Definition:A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.
Synonyms: Carney Complex, Type 1, Carney Complex, Type 2, Carney Syndrome, Carney complex variant, LAMB Syndrome, NAME Syndrome,
Xenbase Genes : prkar1a, myh8
MONDO:0015285 - Carney complex |
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)