restrictive cardiomyopathy
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 ]
Term info
- Orphanet:217632 (MONDO:equivalentTo)
- MESH:D002313 (Orphanet:217632/e)
- SCTID:415295002 (MONDO:equivalentTo)
- MedDRA:10038748 (Orphanet:217632/e)
- ICD9:425.4 (MONDO:relatedTo)
- EFO:0002630 (MONDO:equivalentTo)
- DOID:397 (MONDO:equivalentTo)
- NCIT:C62798 (MONDO:equivalentTo)
- UMLS:C0007196 (Orphanet:217632/e)
disease_grouping, ordo_group_of_disorders
http://identifiers.org/meddra/10038748
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.
http://linkedlifedata.com/resource/umls/id/C0007196, http://purl.obolibrary.org/obo/Orphanet_217632, http://identifiers.org/mesh/D002313, http://identifiers.org/snomedct/415295002, http://purl.obolibrary.org/obo/DOID_397, http://purl.obolibrary.org/obo/NCIT_C62798
primary restrictive cardiomyopathy, restrictive cardiomyopathy, cardiomyopathy, constrictive
familial restrictive cardiomyopathy
MONDO:0005201