Disease #04172

Official abbreviation CM
Name cardiomyopathy (CM)
OMIM ID -
Individuals reported having this disease 103
Phenotype entries for this disease 103
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -


Individuals

103 entries on 2 pages. Showing entries 1 - 100.
Legend   « First ‹ Prev     1 2     Next › Last »

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age/Death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00029119 - DB Barth Syndrome Foundation Bowles (Houston, USA) - M - United States - - 0 Barth Syndrome Foundation - CM see paper; X-linked infantile cardiomyopathy TAZ TAZ 1 1 Johan den Dunnen
00029183 - PubMed: BIssler 2002 4-generation family, 6 affected males, >6 carrier females M - United States - - 0 Barth Syndrome Foundation - CM see paper; X-linked infantile cardiomyopathy TAZ TAZ 2 1 Johan den Dunnen
00029225 - PubMed: D'Adamo 1997, PubMed: van Werkhoven 2006 - M - - - - 0 Barth Syndrome Foundation - CM - TAZ TAZ 1 1 Johan den Dunnen
00029259 - PubMed: D'Adamo 1997 - M - - - - 0 Barth Syndrome Foundation - CM - TAZ TAZ 1 1 Johan den Dunnen
00035617 - - - F - Germany - - 0 - - CM severe cardiomyopathy, suspected DMD-carrier, son has DMD (pathogenic variant DMD-gene) DMD DMD 1 2 Andreas Laner
00053148 - PubMed: Brodehl 2013 4-generation family, 15 affecteds - no United States - - 0 - - CM - DES DES 1 15 Andreas Brodehl
00058003 - - - - - (United States) - - 0 - - CM cardiomyopathy TTN TTN 1 1 Johan den Dunnen
00072985 - - OMIM600857:0004; 1 family 15 affected - - - Bedouin - 0 - - CM familial neonatal isolated cardiomyopathy; 15 Bedouin patients with familial neonatal isolated cardiomyopathy SDHA SDHA 1 1 Jean-Pierre Bayley
00089012 - - 3-generation family, affected mother, daughter (II2, 56y) and grandson (III2, 40y) M no Austria - - 0 - - CM cardiomyopathy, mild LAMP2 LAMP2 3 3 Hakan Cetin
00100912 01570831-Pat PubMed: Saraiva 1992 - - - - - - 0 - - CM Cardiomyopathy TTR TTR 1 1 Johan den Dunnen
00100913 19752327-Pat PubMed: Rapezzi 2009 - - - - - - 0 - - CM Cardiomyopathy TTR TTR 1 1 Johan den Dunnen
00100914 17968689-Pat PubMed: Tarquini 2007 - - - - - - 0 - - CM Cardiomyopathy, late-onset polyneuropathy of lower limbs ? TTR TTR 1 1 Johan den Dunnen
00154714 - PubMed: Fujino 2001 3-generation family, 2 affecteds - no Japan - - 0 - - CM - TNNT2 TNNT2 1 2 Peikuan Cong
00154814 - PubMed: Strijack 2008 family with hypertrophic cardiomyopathy F - Canada white - 0 - - CM extensive, diffuse late gadolinium enhancement left ventricle TNNT2 TNNT2 1 1 Peikuan Cong
00163871 - PubMed: Verhagen 2018, Journal: Verhagen 2018 - ? - Netherlands - - - yes - CM - - CALR3 1 1 Judith Verhagen
00163873 - PubMed: Verhagen 2018, Journal: Verhagen 2018 - ? - Netherlands - - - yes - CM - - CALR3 1 1 Judith Verhagen
00163897 - PubMed: Verhagen 2018, Journal: Verhagen 2018 - M - Netherlands Caucasian - 0 yes - CM - - CALR3 1 1 Judith Verhagen
00163899 - PubMed: Verhagen 2018, Journal: Verhagen 2018 - M - Netherlands Sub-Saharan African - 0 yes implantable cardiac defibrillator CM atrial fibrillation (HP:0005110), paroxysmal ventricular tachycardia (HP:0004751), first degree atrioventricular block (HP:0011705) - CALR3, DES 2 1 Judith Verhagen
00209200 - PubMed: Sen-Chowdhry Left dominant arrhythmogenic cardiomyopathy (LDAC) - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSG2 DSG2 1 1 Paul van der Zwaag
00209339 - PubMed: Sen-Chowdhry Left Dominant Arrhythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 1 Paul van der Zwaag
00209341 - PubMed: Sen-Chowdhry Left Dominant Arrhythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 1 Paul van der Zwaag
00209343 - PubMed: Sen-Chowdhry Left Dominant Arrythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 1 Paul van der Zwaag
00209345 - PubMed: Sen-Chowdhry Left Dominant Arrhythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 1 Paul van der Zwaag
00209349 - PubMed: Sen-Chowdhry Left Dominant Arrhythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 4 Paul van der Zwaag
00209350 - PubMed: Sen-Chowdhry Left Dominant Arrhythmogenic Cardiomyopathy - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy DSP DSP 1 1 Paul van der Zwaag
00209413 - - SCD at age 9; cardiomyopathy, plantar keratoderma, alopecia and bullous dermatosis - - - - - 0 - - CM cardiomyopathy DSP DSP 2 1 Paul van der Zwaag
00209647 - PubMed: Sen-Chowdhry - - - - - - 0 - - CM left-dominant arrhythmogenic cardiomyopathy PKP2 PKP2 1 1 Paul van der Zwaag
00212031 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212039 16715312 PubMed: Zeller 2006 - - - Germany - - 0 - - CM dilated/hypertrophic MYBPC3 MYBPC3 1 1 Peikuan Cong
00212054 11499718 PubMed: Maron 2001 - - - United States - - 0 - - CM - MYBPC3 MYBPC3 1 1 Peikuan Cong
00212116 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212240 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212292 19151713 PubMed: Dhandapany 2009 - - - India - - 0 - - CM 2/3 died as child <3y from cardiomyopathy MYBPC3 MYBPC3 2 3 Johan den Dunnen
00212293 19151713 PubMed: Dhandapany 2009 - - - India - - 0 - - CM - MYBPC3 MYBPC3 1 46 Johan den Dunnen
00212294 19151713 PubMed: Dhandapany 2009 - - - India - - 0 - - CM - MYBPC3 MYBPC3 1 278 Johan den Dunnen
00212313 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212328 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212329 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212372 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212385 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212396 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212399 19858127 PubMed: Tajsharghi 2010 - - - United States - - 0 - - CM - MYBPC3 MYBPC3 1 1 Peikuan Cong
00212422 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212423 16715312 PubMed: Zeller 2006 - - - Germany - - 0 - - CM dilated/hypertrophic MYBPC3 MYBPC3 1 1 Peikuan Cong
00212445 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212456 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212475 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212484 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212490 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212502 18957093 PubMed: Ehlermann 2008 - - - Germany - - 0 - - CM Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. MYBPC3 MYBPC3 1 1 Peikuan Cong
00212504 16715312 PubMed: Zeller 2006 - - - Germany - - 0 - - CM dilated/hypertrophic MYBPC3 MYBPC3 1 1 Peikuan Cong
00212521 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212522 - PubMed: Niimura 1998 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212523 - PubMed: Carrier 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212524 - PubMed: Niimura 1998 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 26 Johan den Dunnen
00212525 - PubMed: Richard 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212526 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212527 - PubMed: Carrier 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212528 - PubMed: Richard 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212529 - PubMed: Bonne 1995 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212530 - PubMed: Richard 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212531 - PubMed: Carrier 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212532 - PubMed: Niimura 1998 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212533 - PubMed: Carrier 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212534 - PubMed: Moolman-Smook 1999 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212535 - PubMed: Richard 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212536 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212537 - PubMed: Richard 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212538 - PubMed: Moolman-Smook 1999 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212539 - PubMed: Kimura 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212540 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212541 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212542 - PubMed: Watkins 1995 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212543 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212544 - PubMed: Rottbauer 1997 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212545 - PubMed: Niimura 1998 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212546 - Sawyer (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212547 - Caramins (Sydney, Australia) July 2003 - - - - - - 0 - - CM - MYBPC3 MYBPC3 1 1 Johan den Dunnen
00212693 - PubMed: Darin 2007 - - - - - - 0 - - CM - MYH7 MYH7 1 1 Johan den Dunnen
00212721 - PubMed: Kaneda 2008 - - - - - - 0 - - CM - MYH7 MYH7 1 1 Johan den Dunnen
00212795 - PubMed: Homayoun 2011 - - - - - - 0 - - CM - MYH7 MYH7 1 1 Johan den Dunnen
00212809 - PubMed: Karam 2008 - - - - - - 0 - - CM - MYH7 MYH7 1 1 Johan den Dunnen
00216922 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
00216923 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
00216924 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 10 Johan den Dunnen
00216925 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 5 Johan den Dunnen
00216926 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
00216927 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
00216928 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 3 Johan den Dunnen
00216929 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 3 Johan den Dunnen
00216930 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 17 Johan den Dunnen
00216931 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 18 Johan den Dunnen
00216932 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 15 Johan den Dunnen
00216933 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 886 Johan den Dunnen
00216934 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 7 Johan den Dunnen
00216935 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 3 Johan den Dunnen
00216936 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 4 Johan den Dunnen
00216937 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
00216938 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 2 Johan den Dunnen
00216939 22286171-pats PubMed: Purevjav 2012 - - - - - - 0 - - CM - MYPN MYPN 1 1 Johan den Dunnen
Legend   « First ‹ Prev     1 2     Next › Last »