MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
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Disease Browser
Parent Node:
expandfamilial dilated cardiomyopathy (MONDO:0016333)
Parent Node:
expandqualitative or quantitative defects of dystrophin (MONDO:0016147)
..Starting node
..expandfamilial isolated dilated cardiomyopathy ()

       Child Nodes:
........expanddilated cardiomyopathy 1A ()
........expanddilated cardiomyopathy 1AA ()
........expanddilated cardiomyopathy 1B ()
........expanddilated cardiomyopathy 1BB ()
........expanddilated cardiomyopathy 1C ()
........expanddilated cardiomyopathy 1CC ()
........expanddilated cardiomyopathy 1D ()
........expanddilated cardiomyopathy 1DD ()
........expanddilated cardiomyopathy 1E ()
........expanddilated cardiomyopathy 1EE ()
........expanddilated cardiomyopathy 1FF ()
........expanddilated cardiomyopathy 1G ()
........expanddilated cardiomyopathy 1GG ()  LSDB  L: 00086;
........expanddilated cardiomyopathy 1H ()
........expanddilated cardiomyopathy 1HH ()
........expanddilated cardiomyopathy 1I ()
........expanddilated cardiomyopathy 1II ()
........expanddilated cardiomyopathy 1JJ ()
........expanddilated cardiomyopathy 1K ()
........expanddilated cardiomyopathy 1L ()
........expanddilated cardiomyopathy 1M ()
........expanddilated cardiomyopathy 1NN ()
........expanddilated cardiomyopathy 1O ()
........expanddilated cardiomyopathy 1P ()
........expanddilated cardiomyopathy 1Q ()
........expanddilated cardiomyopathy 1R ()
........expanddilated cardiomyopathy 1S ()
........expanddilated cardiomyopathy 1T ()
........expanddilated cardiomyopathy 1U ()
........expanddilated cardiomyopathy 1V ()
........expanddilated cardiomyopathy 1W ()
........expanddilated cardiomyopathy 1X ()
........expanddilated cardiomyopathy 1Y ()
........expanddilated cardiomyopathy 1Z ()
........expanddilated cardiomyopathy 2A ()
........expanddilated cardiomyopathy 2B ()
........expanddilated cardiomyopathy 3B ()
........expandleft ventricular noncompaction 10 ()
........expandleft ventricular noncompaction 8 ()



 Sister Nodes: 
..expandfamilial isolated dilated cardiomyopathy ()
..expandisolated asymptomatic elevation of creatine phosphokinase ()
..expandsymptomatic form of muscular dystrophy of Duchenne and Becker in female carriers ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:15470
Name:familial isolated dilated cardiomyopathy
Definition: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.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:familial or idiopathic dilated cardiomyopathy
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal