Familial isolated dilated cardiomyopathy

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Familial isolated dilated cardiomyopathy is a rare, genetically heterogeneous cardiac disease characterized by dilatation leading to systolic and diastolic dysfunction of the left and/or right ventricles, causing heart failure or arrhythmia.

Synonyms: Familial or idiopathic dilated cardiomyopathy

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Term information

database cross reference
hasDbXref

OMIM:302045
OMIM:609915
OMIM:604765
OMIM:601494
OMIM:601154
OMIM:600884
OMIM:604288
OMIM:604145
OMIM:608569
UMLS:C0340427
OMIM:615184
OMIM:115200
OMIM:613122
OMIM:613881
OMIM:613286
OMIM:614672
OMIM:611880
OMIM:612158
OMIM:613642
ICD-10:I42.0
OMIM:615248
OMIM:613424
OMIM:612877
OMIM:613426
OMIM:606685
OMIM:611407
OMIM:601493
OMIM:618189
OMIM:615396
OMIM:613172
OMIM:609909
OMIM:613252
OMIM:615373
OMIM:615235
OMIM:613694
OMIM:613697
OMIM:605582
OMIM:611878
OMIM:607482
OMIM:611879
OMIM:611615
OMIM:615916

notation

ORPHA:154

Term relations

Related from:
disease-causing germline mutation(s) in