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Disease Ontology Browser
Carney complex (DOID:0050471)
Alliance: disease page
Synonyms: Carney complex variant; Carney Complex, Type 1; Carney Complex, Type 2; Carney Syndrome; LAMB Syndrome; NAME Syndrome
Alt IDs: OMIM:160980, OMIM:605244, OMIM:608837, MESH:D056733, NCI:C4705, ORDO:1359, UMLS_CUI:C0406810, UMLS_CUI:C1854540, UMLS_CUI:C2607929
Definition: An autosomal dominant disease characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory