Search Ontology:
Human Disease
renal hypomagnesemia 6
- Term ID
- DOID:0060884
- Synonyms
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- HOMG6
- 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
- References
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- GARD:12155
- ICD10CM:E83.4
- MIM:613882
- ORDO:34527
- Ontology
- Human Disease ( DOID:0060884 )
- is a type of
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