Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/613882 http://purl.bioontology.org/ontology/OMIM/613882
Preferred Name	HYPOMAGNESEMIA 6, RENAL
Synonyms	HOMG6
Type	http://www.w3.org/2002/07/owl#Class

altLabel	HOMG6
prefLabel	HYPOMAGNESEMIA 6, RENAL
Gene Symbol	HOMG6 HOMGSMR ACDP2 CNNM2
Scope Statement	Some people with a CNNM2 mutation are asymptomatic [MISCELLANEOUS] Caused by mutation in the cyclin M2 gene (CNNM2, 607803.0001) [MOLECULAR BASIS] Variable presentation of clinical features [MISCELLANEOUS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU001035 http://purl.bioontology.org/ontology/OMIM/MTHU030492 http://purl.bioontology.org/ontology/OMIM/MTHU004882 http://purl.bioontology.org/ontology/OMIM/MTHU036635 http://purl.bioontology.org/ontology/OMIM/MTHU030493
tui	T047
Gene Locus	10q24.33
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	613882
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C3151295
OMIM Entry Type	3
OMIM MimType Value	pound

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