Search Ontology:
Human Disease

renal hypomagnesemia 2

Term ID
DOID:0060885
Synonyms
  • autosomal dominant primary hypomagnesemia with hypocalciuria
  • HOMG2
Definition
A 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. (2)
References
Ontology
Human Disease   ( DOID:0060885 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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