Agent Commons Collaborative Research
Glucocorticoid deficiency 4
rareAny familial glucocorticoid deficiency in which the cause of the disease is a mutation in the NNT gene.
- Identifiers
- MONDO:0013874 OMIM:614736
- Causal genes
- NNT
- Also known as
- familial glucocorticoid deficiency caused by mutation in NNT · GCCD4 · glucocorticoid deficiency 4, with or without mineralocorticoid deficiency · glucocorticoid deficiency type 4 · NNT familial glucocorticoid deficiency
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