loading...| Preferred Name | dilated cardiomyopathy | |
| Synonyms |
familial dilated cardiomyopathy primary dilated cardiomyopathy idiopathic dilation cardiomyopathy congestive cardiomyopathy Congestive cardiomyopathy Cardiomyopathy, Dilated, with Conduction Deffect1 Primary dilated cardiomyopathy Idiopathic Cardiomyopathy, Familial Familial Idiopathic Cardiomyopathy Cardiomyopathy, Dilated, LMNA Cardiomyopathies, Familial Idiopathic CCM - Congestive cardiomyopathy Familial Idiopathic Cardiomyopathies dilated cardiomyopathy Congestive Cardiomyopathies Congestive cardiomyopathy (disorder) Cardiomyopathy, Congestive Cardiomyopathies, Congestive Cardiomyopathies, Dilated Dilated Cardiomyopathies Idiopathic Cardiomyopathies, Familial Cardiomyopathy, Familial Idiopathic DCM - Dilated cardiomyopathy Congestive dilated cardiomyopathy Cardiomyopathy, Dilated COCM - Congestive cardiomyopathy primary dilated cardiomyopathy (disorder) Cardiomyopathy, Dilated, CMD1A DCM |
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| Definitions |
An intrinsic cardiomyopathy that results in damage to the myocardium causing the heart to pump blood inefficiently. Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure. decreased function of the heart associated with cardiac enlargement and congestive heart failure A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. |
|
| ID |
http://www.ebi.ac.uk/efo/EFO_0000407 |
|
| curated_content_resource |
https://search.clinicalgenome.org/kb/conditions/MONDO:0005021 |
|
| database_cross_reference |
NCIT:C84673 OMIM:615916 SCTID:195021004 MONDO:0005021 OMIM:115200 NANDO:2100057 MedDRA:10056370 OMIM:618189 icd11.foundation:1916294688 MESH:D002311 NANDO:2200232 NCIt:C84673 UMLS:C0007193 MEDGEN:2880 MedDRA:10056419 SNOMEDCT:399020009 ICD10CM:I42.0 Orphanet:217604 MeSH:D002311 DOID:12930 GARD:221 HP:0001644 ICD9:425.4 MP:0002795 |
|
| definition |
An intrinsic cardiomyopathy that results in damage to the myocardium causing the heart to pump blood inefficiently. Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure. decreased function of the heart associated with cardiac enlargement and congestive heart failure A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein. |
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| gwas_trait |
true |
|
| has_exact_synonym |
Congestive cardiomyopathy Cardiomyopathy, Dilated, with Conduction Deffect1 Primary dilated cardiomyopathy Idiopathic Cardiomyopathy, Familial Familial Idiopathic Cardiomyopathy Cardiomyopathy, Dilated, LMNA Cardiomyopathies, Familial Idiopathic CCM - Congestive cardiomyopathy Familial Idiopathic Cardiomyopathies dilated cardiomyopathy Congestive Cardiomyopathies Congestive cardiomyopathy (disorder) Cardiomyopathy, Congestive Cardiomyopathies, Congestive Cardiomyopathies, Dilated Dilated Cardiomyopathies Idiopathic Cardiomyopathies, Familial Cardiomyopathy, Familial Idiopathic DCM - Dilated cardiomyopathy Congestive dilated cardiomyopathy Cardiomyopathy, Dilated COCM - Congestive cardiomyopathy primary dilated cardiomyopathy (disorder) Cardiomyopathy, Dilated, CMD1A DCM |
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| has_related_synonym |
familial dilated cardiomyopathy primary dilated cardiomyopathy idiopathic dilation cardiomyopathy congestive cardiomyopathy |
|
| id |
EFO:0000407 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#clingen http://purl.obolibrary.org/obo/mondo/mondo-base#otar http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping |
|
| label |
dilated cardiomyopathy |
|
| notation |
EFO:0000407 |
|
| preferred label |
dilated cardiomyopathy |
|
| prefLabel |
dilated cardiomyopathy |
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| skos_closeMatch | ||
| skos_exactMatch |
http://purl.bioontology.org/ontology/ICD10CM/I42.0 http://purl.obolibrary.org/obo/EFO_0000407 http://identifiers.org/snomedct/195021004 http://purl.obolibrary.org/obo/NCIT_C84673 http://linkedlifedata.com/resource/umls/id/C0007193 http://purl.obolibrary.org/obo/DOID_12930 http://identifiers.org/medgen/2880 http://identifiers.org/mesh/D002311 http://purl.obolibrary.org/obo/Orphanet_217604 http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1916294688 |
|
| term editor |
Tomasz Adamusiak James Malone |
|
| subClassOf |