Kidney Tissue Atlas Ontology

Last uploaded: March 16, 2024
Preferred Name

familial restrictive cardiomyopathy

Synonyms

hereditary restrictive cardiomyopathy

Definitions

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

ID

http://purl.obolibrary.org/obo/MONDO_0016340

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml

database_cross_reference

Orphanet:217635

SCTID:233878008

ICD9:425.4

OMIMPS:115210

exactMatch

http://linkedlifedata.com/resource/umls/id/C0340429

http://identifiers.org/snomedct/233878008

http://www.orpha.net/ORDO/Orphanet_217635

has exact synonym

hereditary restrictive cardiomyopathy

id

MONDO:0016340

imported from

http://purl.obolibrary.org/obo/mondo.owl

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders

label

familial restrictive cardiomyopathy

notation

MONDO:0016340

prefLabel

familial restrictive cardiomyopathy

should_conform_to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml

textual definition

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

subClassOf

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

http://purl.obolibrary.org/obo/MONDO_0005201

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