familial isolated dilated cardiomyopathy
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
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familial isolated dilated cardiomyopathy
Summary
familial isolated dilated cardiomyopathy is a class of disease[1].
Key Facts
- familial isolated dilated cardiomyopathy's instance of is recorded as class of disease[2].
- familial isolated dilated cardiomyopathy's subclass of is recorded as familial dilated cardiomyopathy[3].
- familial isolated dilated cardiomyopathy's Orphanet ID is recorded as 154[4].
- familial isolated dilated cardiomyopathy's genetic association is recorded as MYH7[5].
- familial isolated dilated cardiomyopathy's genetic association is recorded as MYPN[6].
- familial isolated dilated cardiomyopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_154[7].
- familial isolated dilated cardiomyopathy's UMLS CUI is recorded as C0340427[8].
- familial isolated dilated cardiomyopathy's UMLS CUI is recorded as C5679590[9].
- familial isolated dilated cardiomyopathy's ICD-10-CM is recorded as I42.0[10].
- familial isolated dilated cardiomyopathy's Mondo ID is recorded as MONDO_0015470[11].
- familial isolated dilated cardiomyopathy's ICD-11 ID is recorded as BC43.00[12].
- familial isolated dilated cardiomyopathy's ICD-11 ID is recorded as 423719003[13].