Mondo Disease Ontology

Last uploaded: November 25, 2024
Preferred Name

familial cardiomyopathy
Synonyms

hereditary cardiomyopathy

Definitions

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

ID

http://purl.obolibrary.org/obo/MONDO_0005217

database_cross_reference

UMLS:C0264789

icd11.foundation:1018022925

ICD9:425.4

SCTID:35728003

MEDGEN:538845

EFO:0002945

definition

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

has_exact_synonym

hereditary cardiomyopathy

id

MONDO:0005217

in_subset

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

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

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

label

familial cardiomyopathy

notation

MONDO:0005217

prefLabel

familial cardiomyopathy

skos_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

treeView

http://purl.obolibrary.org/obo/MONDO_0004994

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

subClassOf

http://purl.obolibrary.org/obo/MONDO_0004994

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

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