Search Ontology:
Human Disease
glucocorticoid deficiency 2
- Term ID
- DOID:0061242
- Synonyms
-
- Definition
- A familial glucocorticoid deficiency that has_material_basis_in homozygous mutation in the MRAP gene, encoding melanocortin-2 receptor accessory protein, on chromosome 21q22. https://pubmed.ncbi.nlm.nih.gov/15654338/
- References
- Ontology
- Human Disease ( DOID:0061242 )
Other Pages
Genes Involved
Zebrafish Models