Glucocorticoid Deficiency 1
Disease ID: disease_node_17793
Connections displayed (default: 10).
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| Dbxref | MIM:202200 |
|---|---|
| Subclassof | DOID_0050737, DOID_0080620 |
| Data Source | DOID |
| Doid Label | glucocorticoid deficiency 1 |
| Doid 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. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17793 |
| Doid Id | DOID_0080621 |
| Label | Glucocorticoid Deficiency 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Familial Glucocorticoid Deficiency(ID:disease_node_17792) (Disease)