Search Ontology:
Human Disease
glucocorticoid deficiency 5
- Term ID
- DOID:0061244
- Synonyms
-
- Definition
- A familial glucocorticoid deficiency that has_material_basis_in homozygous mutation in the TXNRD2 gene on chromosome 22q11. https://pubmed.ncbi.nlm.nih.gov/24601690/
- References
- Ontology
- Human Disease ( DOID:0061244 )
Other Pages
Genes Involved
Zebrafish Models