renal hypomagnesemia 3
hypomagnesemia characterized by autosomal recessive inheritance of excessive urinary Ca(2+) and Mg(2+) excretion that has material basis in homozygous or compound heterozygous mutation in the CLDN16 gene on chromosome 3q28
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renal hypomagnesemia 3
Summary
renal hypomagnesemia 3 is a class of disease[1].
Key Facts
- renal hypomagnesemia 3's instance of is recorded as class of disease[2].
- renal hypomagnesemia 3's subclass of is recorded as primary hypomagnesemia[3].
- renal hypomagnesemia 3's subclass of is recorded as renal tubular transport disease[4].
- renal hypomagnesemia 3's subclass of is recorded as familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis[5].
- renal hypomagnesemia 3's MeSH descriptor ID is recorded as C537153[6].
- renal hypomagnesemia 3's OMIM ID is recorded as 248250[7].
- renal hypomagnesemia 3's Disease Ontology ID is recorded as DOID:0060880[8].
- renal hypomagnesemia 3's Orphanet ID is recorded as 31043[9].
- renal hypomagnesemia 3's genetic association is recorded as CLDN16[10].
- renal hypomagnesemia 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060880[11].
- renal hypomagnesemia 3's exact match is recorded as http://identifiers.org/doid/DOID:0060880[12].
- renal hypomagnesemia 3's UMLS CUI is recorded as C0268448[13].
- renal hypomagnesemia 3's UMLS CUI is recorded as C3151482[14].
- renal hypomagnesemia 3's UMLS CUI is recorded as C4511528[15].
- renal hypomagnesemia 3's ICD-10-CM is recorded as E83.4[16].
- renal hypomagnesemia 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- renal hypomagnesemia 3's Mondo ID is recorded as MONDO_0009550[18].
- renal hypomagnesemia 3's UniProt disease ID is recorded as DI-00578[19].