renal hypomagnesemia 2
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
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renal hypomagnesemia 2
Summary
renal hypomagnesemia 2 is a rare disease[1].
Key Facts
- renal hypomagnesemia 2's instance of is recorded as rare disease[2].
- renal hypomagnesemia 2's instance of is recorded as class of disease[3].
- renal hypomagnesemia 2's subclass of is recorded as primary hypomagnesemia[4].
- renal hypomagnesemia 2's subclass of is recorded as familial primary hypomagnesemia with hypocalcuria[5].
- renal hypomagnesemia 2's MeSH descriptor ID is recorded as C537152[6].
- renal hypomagnesemia 2's OMIM ID is recorded as 154020[7].
- renal hypomagnesemia 2's Disease Ontology ID is recorded as DOID:0060885[8].
- renal hypomagnesemia 2's Orphanet ID is recorded as 34528[9].
- renal hypomagnesemia 2's genetic association is recorded as FXYD2[10].
- renal hypomagnesemia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060885[11].
- renal hypomagnesemia 2's exact match is recorded as http://identifiers.org/doid/DOID:0060885[12].
- renal hypomagnesemia 2's exact match is recorded as http://purl.obolibrary.org/obo/HP_0005567[13].
- renal hypomagnesemia 2's UMLS CUI is recorded as C1835171[14].
- renal hypomagnesemia 2's Human Phenotype Ontology ID is recorded as HP:0005567[15].
- renal hypomagnesemia 2's ICD-10-CM is recorded as E83.4[16].
- renal hypomagnesemia 2's GARD rare disease ID is recorded as 3350[17].
- renal hypomagnesemia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- renal hypomagnesemia 2's Mondo ID is recorded as MONDO_0007937[19].
- renal hypomagnesemia 2's UniProt disease ID is recorded as DI-00577[20].