Renal Hypomagnesemia 6
Disease ID: disease_node_17552
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| Dbxref | GARD:12155, ICD10CM:E83.4, MIM:613882, ORDO:34527 |
|---|---|
| Subclassof | DOID_0060879 |
| Data Source | DOID |
| Synonyms | HOMG6 |
| Doid Label | renal hypomagnesemia 6 |
| Doid Description | A hypomagnesemia characterized by autosomal domit inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24. |
| Disease Node Id | disease_node_17552 |
| Doid Id | DOID_0060884 |
| Label | Renal Hypomagnesemia 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Hypomagnesemia(ID:disease_node_17549) (Disease)