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| Term | glucocorticoid deficiency 4 with or without mineralocorticoid deficiency | ID (Ontology) | DOID:0061243 (Human Disease) |
| Definition | A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NNT gene on chromosome 5p12. | ||
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autosomal genetic disease |__autosomal recessive disease_________ adrenal gland disease | |__familial glucocorticoid deficiency__| glucocorticoid deficiency 4 with or without mineralocorticoid deficiency |
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| Is a |
autosomal recessive disease familial glucocorticoid deficiency |
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| MIM:614736 | |||
