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ACTH-independent macronodular adrenal hyperplasia 2

MONDO:0014416

Any Cushing syndrome due to macronodular adrenal hyperplasia in which the cause of the disease is a mutation in the ARMC5 gene.

Also known as: ACTH-independent macronodular adrenal hyperplasia 2, ACTH-independent macronodular adrenal hyperplasia 2, autosomal dominant, somatic mutation, ACTH-independent macronodular adrenal hyperplasia type 2, AIMAH2, ARMC5 Cushing syndrome due to macronodular adrenal hyperplasia, Cushing syndrome due to macronodular adrenal hyperplasia caused by mutation in ARMC5, primary macronodular adrenal hyperplasia

3 clinical trials for this condition and its sub-types, 0 tagged with ACTH-independent macronodular adrenal hyperplasia 2 itself.

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