Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/621270 http://purl.bioontology.org/ontology/OMIM/621270
Preferred Name	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 31
Synonyms	CMH31
Type	http://www.w3.org/2002/07/owl#Class

altLabel	CMH31
prefLabel	CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 31
Gene Symbol	SMRZ RNF28 MURF1 CMH31 TRIM63
Scope Statement	Caused by mutation in the mutation in the tripartite motif containing 63 gene (TRIM63, 606131.0001) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU079886 http://purl.bioontology.org/ontology/OMIM/MTHU079887 http://purl.bioontology.org/ontology/OMIM/MTHU079883 http://purl.bioontology.org/ontology/OMIM/MTHU006040 http://purl.bioontology.org/ontology/OMIM/MTHU034316 http://purl.bioontology.org/ontology/OMIM/MTHU079889 http://purl.bioontology.org/ontology/OMIM/MTHU079888 http://purl.bioontology.org/ontology/OMIM/MTHU068993 http://purl.bioontology.org/ontology/OMIM/MTHU079884 http://purl.bioontology.org/ontology/OMIM/MTHU079885 See more See less
tui	T047
Gene Locus	1p36.11
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	621270
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000016
cui	C6012754
OMIM Entry Type	3
OMIM MimType Value	pound

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