Carney complex, type 1

MONDO:0008057

Any Carney complex in which the cause of the disease is a mutation in the PRKAR1A gene.

Also known as: Carney complex caused by mutation in PRKAR1A, Carney complex, type 1, PRKAR1A Carney complex, CNC1, Carney Myxoma-endocrine Complex, Carney syndrome, lamb syndrome, myxoma, spotty pigmentation, and endocrine overactivity

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Human disease (14) Carney complex (4) Disease of genetic or genomic mechanism (2) Autosomal dominant disease (0) Autosomal genetic disease (0) Disease by etiologic mechanism (0)

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