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About: renal hypomagnesemia 6     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • renal hypomagnesemia 6
described by
id
  • DOID:0060884
database_cross_reference
  • GARD:12155
  • ICD10CM:E83.4
  • OMIM:613882
  • ORDO:34527
has_exact_synonym
  • HOMG6 (en)
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • 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.
is topic of
is annotatedSource of
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