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Metadata
ID DOID:0060884
Name renal hypomagnesemia 6
Definition A hypomagnesemia characterized by autosomal dominant 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.
https://www.ncbi.nlm.nih.gov/pubmed/21397062
Xrefs

GARD:12155

ICD10CM:E83.4

OMIM:613882

ORDO:34527

Subsets

DO_rare_slim

Synonyms

HOMG6 [EXACT]

Parent Relationships

is_a primary hypomagnesemia

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