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Dilated Cardiomyopathy (CUI C0007193) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0007193

NCI Thesaurus Code: C84673  (see NCI Thesaurus info)

Semantic Type: Disease or Syndrome

NCIt Definition: 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.

RADLEX Definition: A form of cardiac muscle disease that is characterized by ventricular dilation, contractile dysfunction of the left or both heart ventricles, and congestive heart failure (heart failure, congestive) symptoms. Risk factors include ethanol and tobacco abuse, pregnancy; hypertension; infection; and mutations in the lmna gene encoding lamin type a, a nuclear lamina protein. [MeSH]

GARD Definition: Dilated cardiomyopathy is a disease of the heart muscle which primarily affects the heart's main pumping chamber, the left ventricle. It is the most common type of cardiomyopathy and typically affects those aged 20 to 60. The left ventricle of affected individuals becomes enlarged (dilated) and cannot pump blood to the body with as much force as a healthy heart can. The heart muscle also has difficulty contracting normally, which can lead to irregular heartbeats (arrhythmia), blood clots, or sudden death. Over time, the heart becomes weaker and heart failure can occur. While the cause of dilated cardiomyopathy is often unknown (idiopathic), some cases are acquired or inherited. - this information is from GARD/ORDR/NCATS.

HPO Definition: Dilated cardiomyopathy (DCM) is defined by the presence of left ventricular dilatation and left ventricular systolic dysfunction in the absence of abnormal loading conditions (hypertension, valve disease) or coronary artery disease sufficient to cause global systolic impairment. Right ventricular dilation and dysfunction may be present but are not necessary for the diagnosis. [pmid:17916581]

MSH 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.

Synonyms & Abbreviations: (see Synonym Details)
Cardiomyopathies, Dilated
Cardiomyopathy, congestive
Cardiomyopathy, Dilated [Disease/Finding]
Cardiomyopathy, dilated
CCM - Congestive cardiomyopathy
COCM - Congestive cardiomyopathy
COCM Congestive (dilated) cardiomyopathy
Congestive (dilated) cardiomyopathy
Congestive cardiomyopathy (disorder)
Congestive cardiomyopathy
Congestive dilated cardiomyopathy
DCM - Dilated cardiomyopathy
DCM
Dilatative Kardiomyopathie
Dilated Cardiomyopathies
dilated cardiomyopathy
Primary dilated cardiomyopathy (disorder)
Primary dilated cardiomyopathy

External Source Codes: 
NCI Thesaurus Code C84673 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN note entry term CARDIOMYOPATHY, CONGESTIVE: do not confuse with HEART FAILURE MSH
AQL BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000017005 SNOMEDCT_US
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID G5544 SNOMEDCT_US
CTV3ID XUYj8 SNOMEDCT_US
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DC 1 MSH
DEFINITION_STATUS_ID 900000000000074008 SNOMEDCT_US
DISEASE_IDENTIFIER_ID 1952 GARD
DX 19860101 MSH
EFFECTIVE_TIME 20020131 SNOMEDCT_US
EFFECTIVE_TIME 20030731 SNOMEDCT_US
HAS_GARD_PAGE true GARD
HN 2005 (1984) MSH
IAN DEFAULT ICD10
IDENTIFIER_TYPE_ID 1 GARD
INCLUSION_TERM Congestive cardiomyopathy ICD10
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
LAST_REVIEW_ACTION Related Disease Added GARD
MDA 19830531 MSH
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. NDFRT
MESH_DUI D002311 NDFRT
MESH_NAME Cardiomyopathy, Dilated NDFRT
MESH_UI M0003463 NDFRT
MMR 20160628 MSH
MN C14.280.195.160 MSH
MN C14.280.238.070 MSH
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Dilated Cardiomyopathy NCI
NUI N0000000686 NDFRT
ORDER_NO 10929 ICD10CM
PM 2005; see CARDIOMYOPATHY, CONGESTIVE 1986-2004, see HEART FAILURE, CONGESTIVE 1984-1985 MSH
PRIMARY_PATH 10056370$10007635$10028593$10007541$Congestive cardiomyopathy$Cardiomyopathies$Myocardial disorders$Cardiac disorders MDR
PRIMARY_SOC 10007541 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/221/dilated-cardiomyopathy/resources/1 GARD
RXAUI 3130536 RXNORM
RXAUI 3130537 RXNORM
RXAUI 3147082 RXNORM
RXCUI 1023271 RXNORM
SID HP:0001725 HPO
SID HP:0005159 HPO
SID HP:0200130 HPO
SMQ_TERM_ADDVERSION 11.1 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 11.1 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 195021004 NDFRT
SNOMED_CID 399020009 NDFRT
SOS A form of cardiomyopathy in which one or more chambers of the heart are abnormally distended with blood. AOD
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS I42.0 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~I42.0 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS I42.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~I42.0 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~G5544 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~XUYj8 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T006640 MSH
TERMUI T006641 MSH
TH UNK (19XX) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0007193

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