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ACTH-independent macronodular adrenal hyperplasia 2
rareAny Cushing syndrome due to macronodular adrenal hyperplasia in which the cause of the disease is a mutation in the ARMC5 gene.
- Identifiers
- MONDO:0014416 OMIM:615954
- Causal genes
- ARMC5
- Also known as
- 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
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