cardiomyopathies

Preferred Label : cardiomyopathies;

MeSH definition : A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS).;

MeSH synonym : myocardial disease; cardiomyopathy; myocardial diseases; disease, myocardial; diseases, myocardial; myocardiopathies; myocardiopathy;

MeSH hyponym : cardiomyopathies, primary; cardiomyopathies, secondary; Cardiomyopathy, Secondary; Secondary Cardiomyopathies; Secondary Cardiomyopathy; Secondary Myocardial Diseases; Disease, Secondary Myocardial; Diseases, Secondary Myocardial; Myocardial Disease, Secondary; Secondary Myocardial Disease; Myocardial Diseases, Secondary; Cardiomyopathy, Primary; Primary Cardiomyopathies; Primary Cardiomyopathy; Primary Myocardial Diseases; Myocardial Diseases, Primary; Disease, Primary Myocardial; Diseases, Primary Myocardial; Myocardial Disease, Primary; Primary Myocardial Disease;

MeSH annotation : GEN; prefer specifics; for infections of the myocardium, coord here (IM) with infection term (IM), not with HEART DISEASES; general or unspecified; prefer specifics; for infections of the myocardium, coordinate here with infection term, not with HEART DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Cardiomyopathy;

Details

Origin ID

D009202;

UMLS CUI

C0878544;

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)
- Cardiomyopathy associated with another disorder (disorder) [SNOMED CT concept]
- Cardiomyopathy primary [MedDRA LLT]
- Cardiomyopathy primary NOS [MedDRA LLT]
- Cardiomyopathy secondary [MedDRA LLT]
- Cardiomyopathy secondary NOS [MedDRA LLT]
- Family History of Cardiomyopathy [NCIt concept]
- MYOCARDIOPATHY [ACR pathology]
- Myocardial degeneration [ICD-10 Sub-category]
- Myocardial disease [PASCAL descriptor]
- Other cardiomyopathies [ICD-10 Sub-category (who)]
- Other primary cardiomyopathies [ICD-9 code]
- Primary cardiomyopathy (disorder) [SNOMED CT concept]
- Secondary cardiomyopathy [ICD-11 More detail]
- Secondary cardiomyopathy, NOS [Inactive SNOMED CT concept]
- Secondary cardiomyopathy, unspecified [ICD-9 code]
- heart disease other [ICPC-2 Rubric]
- myocardial disease, nos [SNOMED Notion]
- myosin heavy chain 6 [HGNC gene]
- primary cardiomyopathy [SNOMED Notion]
- secondary cardiomyopathy, nos [SNOMED Notion]
Currated CISMeF NLP mapping
- CARDIOMYOPATHY [WHO-ART Preferred Term]
- Cardiomyopathies [MedDRA High Level Term]
- Cardiomyopathy [PASCAL descriptor]
- Cardiomyopathy [ICD-10 category]
- Cardiomyopathy [ICD-11 Category]
- Cardiomyopathy [ICD-10 category (who)]
- Cardiomyopathy [HPO term]
- Cardiomyopathy [ICD-9 code]
- Cardiomyopathy [MedDRA Preferred Term]
- Cardiomyopathy [NCIt concept]
- Cardiomyopathy [LOINC component]
- Cardiomyopathy (disorder) [SNOMED CT concept]
- Cardiomyopathy NOS [MedDRA LLT]
- Myocardial disease (disorder) [SNOMED CT concept]
- Rare cardiomyopathy [ORDO Disease]
- cardiomyopathy [DO Concept]
- cardiomyopathy [MedlinePlus Topic]
- cardiomyopathy [Radlex concept]
- cardiomyopathy, nos [SNOMED Notion]
- myocardial disorder [Disease (Nov.)]
DO Cross reference
- cardiomyopathy [DO Concept]
Manual BTNT mappings - CISMeF
- Unclassified cardiomyopathy [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare cardiac disease [ORDO Disease]
MedlinePlus topic(s)
- cardiomyopathy [MedlinePlus Topic]
ORDO relation(s)
- Rare cardiomyopathy [ORDO Disease]
Record concept(s)
- cardiomyopathies [MeSH concept]
- cardiomyopathies, primary [MeSH concept]
- cardiomyopathies, secondary [MeSH concept]
Related MeSH Supplementary Concept(s)
- Alpha-B crystallinopathy [MeSH Supplementary Concept]
- ataxia, deafness, and cardiomyopathy [MeSH Supplementary Concept]
- atrial standstill [MeSH Supplementary Concept]
- cardiac lipidosis, familial [MeSH Supplementary Concept]
- cardiomyopathy associated with myopathy and sudden death [MeSH Supplementary Concept]
- cardiomyopathy dilated with woolly hair and keratoderma [MeSH Supplementary Concept]
- cardiomyopathy hypogonadism collagenoma syndrome [MeSH Supplementary Concept]
- cardiomyopathy, fatal fetal, due to myocardial calcification [MeSH Supplementary Concept]
- cardiomyopathy, infantile histiocytoid [MeSH Supplementary Concept]
- cardioneuromyopathy with hyaline masses and nemaline rods [MeSH Supplementary Concept]
- cataract and cardiomyopathy [MeSH Supplementary Concept]
- encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts [MeSH Supplementary Concept]
- hypertaurinuric cardiomyopathy [MeSH Supplementary Concept]
- keshan disease [MeSH Supplementary Concept]
- muscular dystrophy, cardiac type [MeSH Supplementary Concept]
- myopathy, Early-Onset, with fatal cardiomyopathy [MeSH Supplementary Concept]
- myopathy, myofibrillar, Desmin-Related [MeSH Supplementary Concept]
- najjar syndrome [MeSH Supplementary Concept]
- roifman syndrome [MeSH Supplementary Concept]
- systemic carnitine deficiency [MeSH Supplementary Concept]
- trifunctional protein deficiency with myopathy and neuropathy [MeSH Supplementary Concept]
- uruguay faciocardiomusculoskeletal syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- CARDIOMYOPATHY [WHO-ART Preferred Term]
- Cardiomyopathies [MedDRA High Level Term]
- Cardiomyopathy [MedDRA Preferred Term]
- Cardiomyopathy [LOINC component]
- Cardiomyopathy [ICD-10 category]
- Cardiomyopathy [HPO term]
- Cardiomyopathy [ICD-10 category (who)]
- Cardiomyopathy [ICD-9 code]
- Cardiomyopathy [PASCAL descriptor]
- Cardiomyopathy [NCIt concept]
- Cardiomyopathy (disorder) [SNOMED CT concept]
- Cardiomyopathy NOS [MedDRA LLT]
- Cardiomyopathy, unspecified [ICD-10 Sub-category]
- Myocardial disease (disorder) [SNOMED CT concept]
- Myocardiodystrophy [MedDRA LLT]
- Rare cardiomyopathy [ORDO Disease]
- cardiomyopathy [DO Concept]
- cardiomyopathy [Radlex concept]
- cardiomyopathy [MedlinePlus Topic]
- cardiomyopathy, nos [SNOMED Notion]
- myocardial disease, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- primary myocardial disease [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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