Familial Hypocalciuric Hypercalcemia 2
Disease ID: disease_node_17446
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| Dbxref | GARD:9758, ICD10CM:E83.5, MIM:145981, ORDO:101049 |
|---|---|
| Subclassof | DOID_0060699 |
| Data Source | DOID |
| Synonyms | FHH type 2, HHC2, familial hypocalciuric hypercalcemia type 2, hypocalciuric hypercalcemia type II |
| Doid Label | familial hypocalciuric hypercalcemia 2 |
| Doid Description | A familial hypocalciuric hypercalcemia that has_material_basis_in heterozygous mutation in the GNA11 gene on chromosome 19p13. |
| Disease Node Id | disease_node_17446 |
| Doid Id | DOID_0060701 |
| Label | Familial Hypocalciuric Hypercalcemia 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Familial Hypocalciuric Hypercalcemia(ID:disease_node_17444) (Disease)