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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 complex variant, Carney Syndrome, LAMB Syndrome, NAME Syndrome
Xenbase Genes
:
prkar1a,
myh8
| MONDO:0015285 - Carney complex |
| MIM:160980 - CARNEY COMPLEX, TYPE 1; CNC1 |
| MIM:605244 - CARNEY COMPLEX, TYPE 2; CNC2 |
| 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)