Search Ontology:
Human Disease

renal hypomagnesemia 6

Term ID
DOID:0060884
Synonyms
  • 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
Ontology
Human Disease   ( DOID:0060884 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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