Combined Pituitary Hormone Deficiency 2
Disease ID: disease_node_19691
Connections displayed (default: 10).
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| Dbxref | MIM:262600 |
|---|---|
| Subclassof | DOID_9410, DOID_0050737 |
| Data Source | DOID |
| Synonyms | CPHD2 |
| Doid Label | combined pituitary hormone deficiency 2 |
| Doid Description | A combined pituitary hormone deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the PROP1 gene on chromosome 5q35. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19691 |
| Doid Id | DOID_0061020 |
| Label | Combined Pituitary Hormone Deficiency 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)