Cardiomyopathy, Restrictive
Disease ID: disease_node_1869
Connections displayed (default: 10).
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| Dbxref | ICD10CM:I42.5, MESH:D002313, MIM:115210, MIM:PS115210, NCI:C62798, ORDO:75249, SNOMEDCT_US_2023_03_01:389996009, UMLS_CUI:C0007196 |
|---|---|
| Subclassof | DOID_0060036 |
| Data Source | DOID, MESH |
| Synonyms | Cardiomyopathy, constrictive, primary restrictive cardiomyopathy, Familial restrictive cardiomyopathy |
| Mesh Id | D002313 |
| Mesh Label | Cardiomyopathy, Restrictive |
| Mesh Subclassof | D009202 |
| Doid Label | restrictive cardiomyopathy |
| Doid Description | An intrinsic cardiomyopathy characterized by impaired ventricular filling, with normal or decreased diastolic volume of either or both ventricles typically resulting from increased stiffness of the myocardium. Xref MGI. OMIM mappings 115210, 612422 added from NeuroDevNet [WAK]. |
| Disease Node Id | disease_node_1869 |
| Doid Id | DOID_397 |
| Label | Cardiomyopathy, Restrictive |
- Incoming r'ship
SUBCLASS_OFto/from Loeffler Endocarditis(ID:disease_node_16870) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Restrictive Cardiomyopathy 6(ID:disease_node_16874) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Restrictive Cardiomyopathy 3(ID:disease_node_16871) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Restrictive Cardiomyopathy 1(ID:disease_node_16873) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Restrictive Cardiomyopathy 2(ID:disease_node_16872) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Endomyocardial Fibrosis(ID:disease_node_2931) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Intrinsic Cardiomyopathy(ID:disease_node_16869) (Disease)