Metadata | |
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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 | |
Subsets |
DO_rare_slim |
Synonyms |
autosomal dominant primary hypomagnesemia with hypocalciuria [EXACT] HOMG2 [EXACT] |
Parent Relationships |