JSON

familial dilated cardiomyopathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0016333

A a genetic form of heart disease that occurs when heart (cardiac) muscle becomes thin and weakened in at least one chamber of the heart, causing the open area of the chamber to become enlarged (dilated). As a result, the heart is unable to pump blood as efficiently as usual. To compensate, the heart attempts to increase the amount of blood being pumped through the heart, leading to further thinning and weakening of the cardiac muscle. Over time, this condition results in heart failure. [ https://ghr.nlm.nih.gov/condition/familial-dilated-cardiomyopathy ]

Synonyms: hereditary dilated cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0340427 (MONDO:equivalentTo)
  • MESH:C536231 (Orphanet:217607/e)
  • OMIMPS:115200 (MONDO:equivalentTo)
  • GARD:20525 (MONDO:GARD)
  • Orphanet:217607 (MONDO:equivalentTo)
  • MEDGEN:90951 (MONDO:equivalentTo)
Subsets

gard_rare, otar, disease_grouping, rare, ordo_group_of_disorders

abbreviation
DCM [ GARD:0000221 ]

comment

Editor note: unsure if GARD is familial form

exactMatch

http://linkedlifedata.com/resource/umls/id/C0340427

http://identifiers.org/medgen/90951

http://identifiers.org/mesh/C536231

https://omim.org/phenotypicSeries/PS115200

http://www.orpha.net/ORDO/Orphanet_217607

has related synonym

dilated cardiomyopathy, familial

idiopathic dilated cardiomyopathy

hypokinetic dilated cardiomyopathy, familial

DCM

id

MONDO:0016333

should conform to

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