A type of heart disorder referring to the inability of the ventricles to fill with blood because the myocardium (heart muscle) stiffens and looses its flexibility. Causes include replacement of the myocardium with scar tissue, abnormal cellular infiltration of the myocardium, or deposition of a substance (e.g., amyloid) in the myocardium. [ NCIT:C62798 ]

Synonyms: primary restrictive cardiomyopathy cardiomyopathy, constrictive restrictive cardiomyopathy

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:425.4 (MONDO:relatedTo)
  • MEDGEN:40111 (MONDO:equivalentTo)
  • DOID:397 (MONDO:equivalentTo)
  • UMLS:C0007196 (MONDO:equivalentTo)
  • Orphanet:217632 (MONDO:equivalentTo)
  • NCIT:C62798 (MONDO:equivalentTo)
  • EFO:0002630 (MONDO:equivalentTo)
  • MedDRA:10038748 (Orphanet:217632/e)
  • icd11.foundation:316495940 (Orphanet:217632)
  • SCTID:415295002 (MONDO:equivalentTo)
  • GARD:20531 (MONDO:GARD)
  • NANDO:2100058 (https://orcid.org/0000-0003-0011-764X)
  • NANDO:1200292 (https://orcid.org/0000-0003-0011-764X)
  • MESH:D002313 (Orphanet:217632/e)
  • NANDO:1200293 (https://orcid.org/0000-0003-0011-764X)
  • NANDO:2200233 (https://orcid.org/0000-0003-0011-764X)
Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10038748

exactMatch

http://identifiers.org/medgen/40111

http://linkedlifedata.com/resource/umls/id/C0007196

http://identifiers.org/mesh/D002313

http://www.orpha.net/ORDO/Orphanet_217632

http://identifiers.org/snomedct/415295002

http://purl.obolibrary.org/obo/NCIT_C62798

http://purl.obolibrary.org/obo/DOID_397

has narrow synonym

familial restrictive cardiomyopathy

id

MONDO:0005201

Term relations