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Results 1 - 7 of 7 for Arrhythmogenic right ventricular "dysplasia," "familial," 3
  1. Arrhythmogenic right ventricular cardiomyopathy 
    ... gov ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 3; ARVD3 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 4; ARVD4 ...
    https://medlineplus.gov/...hmogenic-right-ventricular-cardiomyopathy - Genetics
  2. JUP gene 
    ... associated protein), gamma 80kDa CTNNG desmoplakin III desmoplakin-3 DP3 DPIII PDGB PKGB plakoglobin Tests of JUP PubMed JUNCTION PLAKOGLOBIN; JUP ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 12; ARVD12 NCBI Gene ClinVar Asimaki A, Syrris ...
    https://medlineplus.gov/genetics/gene/jup - Genetics
  3. DSC2 gene 
    ... DSC3 Tests of DSC2 PubMed DESMOCOLLIN 2; DSC2 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11; ARVD11 NCBI Gene ClinVar De Bortoli M, Beffagna G, Bauce B, Lorenzon A, Smaniotto G, Rigato I, Calore M, Li Mura ... in arrhythmogenic right ventricular cardiomyopathy. Eur J Hum Genet. 2010 ...
    https://medlineplus.gov/genetics/gene/dsc2 - Genetics
  4. DSP gene 
    ... CARDIOMYOPATHY, DILATED, WITH WOOLLY HAIR AND KERATODERMA; DCWHK ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 8; ARVD8 EPIDERMOLYSIS BULLOSA, LETHAL ACANTHOLYTIC; EBLA CARDIOMYOPATHY, ...
    https://medlineplus.gov/genetics/gene/dsp - Genetics
  5. PKP2 gene 
    ... Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circulation. 2006 Apr 4;113(13):1650- ...
    https://medlineplus.gov/genetics/gene/pkp2 - Genetics
  6. Patient support and advocacy groups 
    ... 1 Foundation ARPKD/CHF Alliance Arrhythmia Alliance (UK) Arrhythmogenic ... Association Barth Syndrome Foundation Batten Disease Family Association ( ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  7. LMNA gene 
    ... the LMNA gene have been found to cause familial partial lipodystrophy type 2 (also known as familial partial lipodystrophy, Dunnigan type), a rare condition characterized ...
    https://medlineplus.gov/genetics/gene/lmna - Genetics