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Carney complex, type 1
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any Carney complex in which the cause of the disease is a mutation in the PRKAR1A gene.
Uniprot Description CNC is a multiple neoplasia syndrome characterized by spotty skin pigmentation, cardiac and other myxomas, endocrine tumors, and psammomatous melanotic schwannomas.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:160980
MONDO:0008057
High level summary of knowledge for a disease, including descriptions and datasource references.