glucocorticoid deficiency 1
Information
- Disease name
- glucocorticoid deficiency 1
- Disease ID
- DOID:0080621
- Description
- "A familial glucocorticoid deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding melanocortin-2 receptor, which is also referred to as adrenocorticotropin receptor, on chromosome 18p11." [url:https\://www.ncbi.nlm.nih.gov/pubmed/19500760]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0080620
- Cross Reference ID (Disease Ontology)
- MIM:202200