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familial primary hypomagnesemia

^ http://purl.obolibrary.org/obo/MONDO_0018100

A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration. [ NCIT:C123263 ]

Term info

database cross reference
  • SCTID:80710001 (MONDO:equivalentTo)
  • NCIT:C123263 (MONDO:equivalentTo)
  • Orphanet:34526 (MONDO:equivalentObsolete)
  • DOID:0060879 (MONDO:equivalentTo)
  • OMIMPS:602014 (MONDO:equivalentTo)
  • GARD:0002906 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

abbreviation
HOMG [ DOID:0060879 ]

definition

A hereditary disorder that leads to a selective defect in renal or intestinal magnesium absorption, resulting in a low serum magnesium concentration.

exactMatch

http://identifiers.org/snomedct/80710001, http://purl.obolibrary.org/obo/DOID_0060879, http://purl.obolibrary.org/obo/NCIT_C123263, https://omim.org/phenotypicSeries/PS602014

has broad synonym

hypomagnesemia

has exact synonym

HOMG, familial primary hypomagnesemia, primary familial hypomagnesemia

id

MONDO:0018100