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familial primary hypomagnesemia

Go to external page 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 ]

Synonyms: HOMG familial primary hypomagnesemia primary familial hypomagnesemia

This is just here as a test because I lose it

Term information

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

disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://purl.obolibrary.org/obo/DOID_0060879

http://identifiers.org/snomedct/80710001

http://purl.obolibrary.org/obo/NCIT_C123263

https://omim.org/phenotypicSeries/PS602014

has broad synonym

hypomagnesemia

id

MONDO:0018100