OBO ID: DOID:0060884
Term Name: renal hypomagnesemia 6 Search Ontology:
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)
OTHER renal hypomagnesemia 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CNNM2 Hypomagnesemia 6, renal 613882
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None