Agent Commons Collaborative Research
Glucocorticoid deficiency 1
rareAny familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MC2R gene.
- Identifiers
- MONDO:0024536 OMIM:202200
- Causal genes
- MC2R
- Also known as
- familial glucocorticoid deficiency caused by mutation in MC2R · GCCD1 · glucocorticoid deficiency, due to ACTH unresponsiveness · MC2R familial glucocorticoid deficiency
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