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
Term information
- 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)
gard_rare, otar, disease_grouping, rare, nord_rare, ordo_group_of_disorders
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