cardiomyopathy, dilated

Preferred Label : cardiomyopathy, dilated;

MeSH definition : 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.;

MeSH synonym : dilated cardiomyopathy; dilated cardiomyopathies; cardiomyopathies, dilated;

CISMeF synonym : 1A, dilated cardiomyopathy;

MeSH hyponym : cardiomyopathy, familial idiopathic; Cardiomyopathies, Familial Idiopathic; Familial Idiopathic Cardiomyopathies; Familial Idiopathic Cardiomyopathy; Idiopathic Cardiomyopathies, Familial; Idiopathic Cardiomyopathy, Familial; Cardiomyopathy, Congestive; Cardiomyopathies, Congestive; Congestive Cardiomyopathies; Cardiomyopathy, Dilated, with Conduction Deffect1; Cardiomyopathy, Dilated, CMD1A; Dilated cardiomyopathy 1A; 1As, Dilated cardiomyopathy; Dilated cardiomyopathy 1As; cardiomyopathy 1A, Dilated; cardiomyopathy 1As, Dilated; Cardiomyopathy, Dilated, Autosomal Recessive; Cardiomyopathy, Dilated, 1a; Cardiomyopathy, Dilated, With Conduction Defect 1; Cardiomyopathy, Idiopathic Dilated; Cardiomyopathies, Idiopathic Dilated; Dilated Cardiomyopathies, Idiopathic; Dilated Cardiomyopathy, Idiopathic; Idiopathic Dilated Cardiomyopathies; Idiopathic Dilated Cardiomyopathy; Congestive Cardiomyopathy; Cardiomyopathy, Dilated, LMNA;

MeSH annotation : note entry term CARDIOMYOPATHY, CONGESTIVE: do not confuse with HEART FAILURE;

Details

Origin ID

D002311;

UMLS CUI

C0007193;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Campomelic Dysplasia [NCIt concept]
- Cardiomyopathy, dilated, 1a [OMIM Phenotype]
- Cardiomyopathy, dilated, 2a [OMIM Phenotype]
- Congenital muscular dystrophy [ORDO Disease]
- Congestive cardiomyopathy [HPO term]
- Coronary Microvascular Disease [NCIt concept]
- Craniometaphyseal dysplasia, autosomal dominant [OMIM Phenotype]
- Dilated Cardiomyopathy Pathway [NCIt concept]
- Dilated cardiomyopathy may be present [HPO term]
- Familial cardiomyopathy [ICD-11 More detail]
- Familial dilated cardiomyopathy [ORDO Disease]
- Microvascular angina [ICD-11 More detail]
- Primary familial dilated cardiomyopathy (disorder) [SNOMED CT concept]
- cardiomyopathy [MedlinePlus Topic]
CISMeF manual mappings
- Primary dilated cardiomyopathy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Congestive (dilated) cardiomyopathy [MedDRA LLT]
- Congestive cardiomyopathy [MedDRA Preferred Term]
- Congestive cardiomyopathy (disorder) [SNOMED CT concept]
- Dilated Cardiomyopathy [NCIt concept]
- Dilated cardiomyopathy [PASCAL descriptor]
- Dilated cardiomyopathy [ICD-10 Sub-category]
- Dilated cardiomyopathy [ICD-11 Subcategory]
- Dilated cardiomyopathy [HPO term]
- Dilated cardiomyopathy [OMIM phenotypic series]
- Dilated cardiomyopathy [ICD-10 Sub-category (who)]
- Dilated cardiomyopathy [ORDO Disease]
- Dilated cardiomyopathy [MedDRA LLT]
- Familial-genetic dilated cardiomyopathy [ICD-11 Sub-sub category]
- Nonobstructive cardiomyopathy (disorder) [SNOMED CT concept]
- congestive cardiomyopathy [SNOMED Notion]
- dilated cardiomyopathy [DO Concept]
- dilated cardiomyopathy [Disease (Nov.)]
- dilated cardiomyopathy [Radlex concept]
- nonobstructive cardiomyopathy [SNOMED Notion]
DO Cross reference
- dilated cardiomyopathy [DO Concept]
False automatic mappings
- His bundle tachycardia [ORDO Disease]
HPO term
- Dilated cardiomyopathy [HPO term]
Indexing information
- FKTN protein, human [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Endocardial fibroelastosis [ORDO Disease]
- Familial isolated dilated cardiomyopathy [ORDO Disease]
- Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy [ORDO Disease]
- HEC syndrome [ORDO Disease]
- Mitochondrial disease with dilated cardiomyopathy [ORDO Disease]
- Neuromuscular disease with dilated cardiomyopathy [ORDO Disease]
- Non-familial dilated cardiomyopathy [ORDO Disease]
- Nuclear cell envelopathy [ORDO Disease]
- Rare genetic cardiac disease [ORDO Disease]
- Severe dilated cardiomyopathy due to lamin A/C mutation [ORDO Disease]
- Syndrome associated with dilated cardiomyopathy [ORDO Disease]
ORDO relation(s)
- Dilated cardiomyopathy [ORDO Disease]
Record concept(s)
- cardiomyopathy, dilated [MeSH concept]
- cardiomyopathy, familial idiopathic [MeSH concept]
Related MeSH Supplementary Concept(s)
- 3-Methylglutaconic aciduria, type V [MeSH Supplementary Concept]
- Dmd-Associated dilated cardiomyopathy [MeSH Supplementary Concept]
- cardiomyopathy dilated with woolly hair and keratoderma [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1AA [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1BB [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1C [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1CC [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1D [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1DD [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1E [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1EE [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1FF [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1J [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1K [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1M [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1N [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1V [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1g [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1i [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1l [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1o [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1p [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1q [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1s [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1t [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1u [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1w [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1x [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1y [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1z [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 2a [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 3A [MeSH Supplementary Concept]
- cardiomyopathy, dilated, with left ventricular noncompaction [MeSH Supplementary Concept]
- cardiomyopathy, right ventricular dilated [MeSH Supplementary Concept]
- familial dilated cardiomyopathy [MeSH Supplementary Concept]
- idiopathic dilation cardiomyopathy [MeSH Supplementary Concept]
- krasnow qazi syndrome [MeSH Supplementary Concept]
- malouf syndrome [MeSH Supplementary Concept]
- uhl anomaly [MeSH Supplementary Concept]
- winship viljoen leary syndrome [MeSH Supplementary Concept]
SNOMED CT : Morphologiquement associé
- dilatation, pathologic [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congestive (dilated) cardiomyopathy [MedDRA LLT]
- Congestive cardiomyopathy [MedDRA Preferred Term]
- Congestive cardiomyopathy [MedDRA LLT]
- Congestive cardiomyopathy (disorder) [SNOMED CT concept]
- Dilated Cardiomyopathy [NCIt concept]
- Dilated cardiomyopathy [ORDO Disease]
- Dilated cardiomyopathy [ICD-10 Sub-category]
- Dilated cardiomyopathy [HPO term]
- Dilated cardiomyopathy [ICD-10 Sub-category (who)]
- Dilated cardiomyopathy [PASCAL descriptor]
- Dilated cardiomyopathy [ICD-11 Subcategory]
- Dilated cardiomyopathy [MedDRA Preferred Term]
- Dilated cardiomyopathy [MedDRA LLT]
- Familial-genetic dilated cardiomyopathy [ICD-11 Sub-sub category]
- Primary dilated cardiomyopathy (disorder) [SNOMED CT concept]
- congestive cardiomyopathy [SNOMED Notion]
- dilated cardiomyopathy [DO Concept]
- dilated cardiomyopathy [Radlex concept]
- dilated cardiomyopathy [Disease (Nov.)]
Validated automatic mappings to BTNT
- dilated cardiomyopathy 1A [DO Concept]
- primary idiopathic dilated cardiomyopathy [Disease (Nov.)]

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