Familial Hypocalciuric Hypercalcemia 3
Disease ID: disease_node_17445
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:2878, ICD10CM:E83.5, MIM:600740, ORDO:101050 |
|---|---|
| Subclassof | DOID_0060699 |
| Data Source | DOID |
| Synonyms | FHH type 3, HHC3, familial hypocalciuric hypercalcemia type 3, hypocalciuric hypercalcemia type III |
| Doid Label | familial hypocalciuric hypercalcemia 3 |
| Doid Description | A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the AP2S1 gene on chromosome 19q13. |
| Disease Node Id | disease_node_17445 |
| Doid Id | DOID_0060702 |
| Label | Familial Hypocalciuric Hypercalcemia 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Familial Hypocalciuric Hypercalcemia(ID:disease_node_17444) (Disease)