Renal Hypomagnesemia 2
Disease ID: disease_node_17551
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| Dbxref | GARD:3350, ICD10CM:E83.4, MIM:154020, ORDO:34528 |
|---|---|
| Subclassof | DOID_0060879 |
| Data Source | DOID |
| Synonyms | HOMG2, autosomal dominant primary hypomagnesemia with hypocalciuria |
| Doid Label | renal hypomagnesemia 2 |
| Doid Description | A hypomagnesemia characterized by autosomal domit inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23. |
| Disease Node Id | disease_node_17551 |
| Doid Id | DOID_0060885 |
| Label | Renal Hypomagnesemia 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Hypomagnesemia(ID:disease_node_17549) (Disease)