Experimental Factor Ontology

Last uploaded: November 18, 2024
Preferred Name

familial cardiomyopathy
Synonyms

familial cardiomyopathy

Primary familial cardiomyopathy

hereditary cardiomyopathy

Familial cardiomyopathy (disorder)

Definitions

An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.

ID

http://www.ebi.ac.uk/efo/EFO_0002945

database_cross_reference

UMLS:C0264789

icd11.foundation:1018022925

MEDGEN:538845

OMIM:115200

SNOMEDCT:35728003

SCTID:35728003

MONDO:0005217

ICD9:425.4

definition

An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome.

exactMatch

http://purl.obolibrary.org/obo/EFO_0002945

http://linkedlifedata.com/resource/umls/id/C0264789

http://identifiers.org/medgen/538845

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1018022925

http://identifiers.org/snomedct/35728003

has_exact_synonym

familial cardiomyopathy

Primary familial cardiomyopathy

hereditary cardiomyopathy

Familial cardiomyopathy (disorder)

id

EFO:0002945

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

label

familial cardiomyopathy

notation

EFO:0002945

preferred label

familial cardiomyopathy

prefLabel

familial cardiomyopathy

term editor

Tomasz Adamusiak

subClassOf

http://www.ebi.ac.uk/efo/EFO_0000318

http://purl.obolibrary.org/obo/MONDO_0100547

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