Search Ontology:
Human Disease
glucocorticoid deficiency 4 with or without mineralocorticoid deficiency
- Term ID
- DOID:0061243
- Synonyms
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- Definition
- A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NNT gene on chromosome 5p12. https://pubmed.ncbi.nlm.nih.gov/22634753/
- References
- Ontology
- Human Disease ( DOID:0061243 )
Other Pages
Genes Involved
Zebrafish Models