Intestinal Hypomagnesemia 1
Disease ID: disease_node_17553
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:E83.4, MIM:602014, ORDO:30924 |
|---|---|
| Subclassof | DOID_0060879 |
| Data Source | DOID |
| Synonyms | HOMG1, hypomagnesemia caused by selective magnesium malabsorption, hypomagnesemia intestinal type 1, hypomagnesemic tetany, intestinal hypomagnesemia with secondary hypocalcemia, primary hypomagnesemia with secondary hypocalcemia |
| Doid Label | intestinal hypomagnesemia 1 |
| Doid Description | A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorption and kidney excretion and secondary hypocalcemia that has_material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21. |
| Disease Node Id | disease_node_17553 |
| Doid Id | DOID_0060883 |
| Label | Intestinal Hypomagnesemia 1 |
- Outgoing r'ship
SUBCLASS_OFto/from Primary Hypomagnesemia(ID:disease_node_17549) (Disease)