Familial Hypocalciuric Hypercalcemia
Disease ID: disease_node_17444
Connections displayed (default: 10).
Loading graph...
| Dbxref | GARD:10828, ICD10CM:E83.5, MIM:PS145980, ORDO:405 |
|---|---|
| Subclassof | DOID_0050736, DOID_12678, DOID_655 |
| Data Source | DOID |
| Synonyms | FBH, FBHH, FHH, familial benign hypercalcemia, familial benign hypocalciuric hypercalcemia |
| Doid Label | familial hypocalciuric hypercalcemia |
| Doid Description | A hypercalcemia characterized by autosomal domit inheritance with elevation of serum calcium levels and decreased urinary calcium excretion. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17444 |
| Doid Id | DOID_0060699 |
| Label | Familial Hypocalciuric Hypercalcemia |
- Incoming r'ship
SUBCLASS_OFto/from Familial Hypocalciuric Hypercalcemia 1(ID:disease_node_17447) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hypercalcemia(ID:disease_node_4079) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Hypocalciuric Hypercalcemia 2(ID:disease_node_17446) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Hypocalciuric Hypercalcemia 3(ID:disease_node_17445) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)