Carney complex, type 1
MONDO:0008057Any 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, 0 tagged with Carney complex, type 1 itself.
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