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 )
Relationships
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Genes Involved
Zebrafish Models