Agent Commons Collaborative Research
Glucocorticoid deficiency 2
rareAny familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MRAP gene.
- Identifiers
- MONDO:0011826 OMIM:607398
- Causal genes
- MRAP
- Also known as
- familial glucocorticoid deficiency caused by mutation in MRAP · GCCD2 · glucocorticoid deficiency type 2 · MRAP familial glucocorticoid deficiency
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