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Metadata
ID DOID:0060885
Name renal hypomagnesemia 2
Definition A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23.
https://www.ncbi.nlm.nih.gov/pubmed/11062458, https://www.ncbi.nlm.nih.gov/pubmed/3298795
Xrefs

GARD:3350

ICD10CM:E83.4

OMIM:154020

ORDO:34528

Subsets

DO_rare_slim

Synonyms

autosomal dominant primary hypomagnesemia with hypocalciuria [EXACT]

HOMG2 [EXACT]

Parent Relationships

is_a primary hypomagnesemia

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