Phenotypes for disease #04172 (CM (cardiomyopathy (CM)))

2213 entries on 23 pages. Showing entries 1 - 100.
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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000025153 see paper; X-linked infantile cardiomyopathy - - Unknown - - - - - Johan den Dunnen 00029119
0000025217 see paper; X-linked infantile cardiomyopathy - - Familial, X-linked recessive - - - - - Johan den Dunnen 00029183
0000025259 - - - Unknown - - - - - Johan den Dunnen 00029225
0000025293 - - - Familial - - - - - Johan den Dunnen 00029259
0000039850 - - - Familial, autosomal dominant - - - - - Andreas Brodehl 00053148
0000044634 cardiomyopathy - - Unknown - - - - - Johan den Dunnen 00058003
0000052676 familial neonatal isolated cardiomyopathy; 15 Bedouin patients with familial neonatal isolated cardiomyopathy - - Unknown - - - - - Jean-Pierre Bayley 00072985
0000068416 cardiomyopathy, mild - - Familial, X-linked dominant - - - - - Hakan Cetin 00089012
0000079131 Cardiomyopathy - - Familial, autosomal dominant - - - - - Johan den Dunnen 00100912
0000079132 Cardiomyopathy - - Familial, autosomal dominant - - - - - Johan den Dunnen 00100913
0000079133 Cardiomyopathy, late-onset polyneuropathy of lower limbs ? - - Familial, autosomal dominant - - - - - Johan den Dunnen 00100914
0000081979 severe cardiomyopathy, suspected DMD-carrier, son has DMD (pathogenic variant DMD-gene) - - Unknown - - - - - Andreas Laner 00035617
0000127450 - cardiomyopathy - Familial - - - - - Peikuan Cong 00154714
0000127550 extensive, diffuse late gadolinium enhancement left ventricle cardiomyopathy - Familial - - - - - Peikuan Cong 00154814
0000128983 - - - Unknown - - - - - Judith Verhagen 00163871
0000128985 - - - Unknown - - - - - Judith Verhagen 00163873
0000129009 - - - Isolated (sporadic) - 82y - - - Judith Verhagen 00163897
0000129011 atrial fibrillation (HP:0005110), paroxysmal ventricular tachycardia (HP:0004751), first degree atrioventricular block (HP:0011705) - - Isolated (sporadic) - 53y - - - Judith Verhagen 00163899
0000157806 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy CMD-1BB Unknown - - - - - Paul van der Zwaag 00209200
0000157938 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209339
0000157940 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209341
0000157942 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209343
0000157944 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209345
0000157948 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209349
0000157949 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209350
0000158012 cardiomyopathy cardiomyopathy - Unknown - - - - - Paul van der Zwaag 00209413
0000158246 left-dominant arrhythmogenic cardiomyopathy left-dominant arrhythmogenic cardiomyopathy ARVD-9 Unknown - - - - - Paul van der Zwaag 00209647
0000160513 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212031
0000160521 dilated/hypertrophic cardiomyopathy CMH-4 Unknown - - - - - Peikuan Cong 00212039
0000160536 - cardiomyopathy, hpertrophic, left ventricular - Unknown - - - - - Peikuan Cong 00212054
0000160598 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212116
0000160722 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212240
0000160774 2/3 died as child <3y from cardiomyopathy cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212292
0000160775 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212293
0000160776 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212294
0000160795 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212313
0000160810 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212328
0000160811 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212329
0000160854 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212372
0000160867 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212385
0000160878 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212396
0000160881 - cardiomyopathy CMH-4 Familial - - - - - Peikuan Cong 00212399
0000160904 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212422
0000160905 dilated/hypertrophic cardiomyopathy CMH-4 Unknown - - - - - Peikuan Cong 00212423
0000160927 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212445
0000160938 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212456
0000160957 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212475
0000160966 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212484
0000160972 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212490
0000160984 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. cardiomyopathy, dilated/hypertrophic - Unknown - - - - - Peikuan Cong 00212502
0000160986 dilated/hypertrophic cardiomyopathy CMH-4 Unknown - - - - - Peikuan Cong 00212504
0000161003 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212521
0000161004 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212522
0000161005 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212523
0000161006 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212524
0000161007 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212525
0000161008 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212526
0000161009 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212527
0000161010 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212528
0000161011 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212529
0000161012 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212530
0000161013 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212531
0000161014 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212532
0000161015 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212533
0000161016 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212534
0000161017 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212535
0000161018 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212536
0000161019 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212537
0000161020 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212538
0000161021 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212539
0000161022 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212540
0000161023 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212541
0000161024 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212542
0000161025 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212543
0000161026 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212544
0000161027 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212545
0000161028 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212546
0000161029 - cardiomyopathy CMH-4 Unknown - - - - - Johan den Dunnen 00212547
0000161175 - cardiomyopathy; myopathy, distal - Unknown - - - - - Johan den Dunnen 00212693
0000161203 - cardiomyopathy CMH-1 Unknown - - - - - Johan den Dunnen 00212721
0000161277 - cardiomyopathy; myopathy, distal - Unknown - - - - - Johan den Dunnen 00212795
0000161291 - cardiomyopathy CMH-1 Unknown - - - - - Johan den Dunnen 00212809
0000165373 - cardiomyopathy - - - - - - - Johan den Dunnen 00216922
0000165374 - cardiomyopathy - - - - - - - Johan den Dunnen 00216923
0000165375 - cardiomyopathy - - - - - - - Johan den Dunnen 00216924
0000165376 - cardiomyopathy - - - - - - - Johan den Dunnen 00216925
0000165377 - cardiomyopathy - - - - - - - Johan den Dunnen 00216926
0000165378 - cardiomyopathy - - - - - - - Johan den Dunnen 00216927
0000165379 - cardiomyopathy - - - - - - - Johan den Dunnen 00216928
0000165380 - cardiomyopathy - - - - - - - Johan den Dunnen 00216929
0000165381 - cardiomyopathy - - - - - - - Johan den Dunnen 00216930
0000165382 - cardiomyopathy - - - - - - - Johan den Dunnen 00216931
0000165383 - cardiomyopathy - - - - - - - Johan den Dunnen 00216932
0000165384 - cardiomyopathy - - - - - - - Johan den Dunnen 00216933
0000165385 - cardiomyopathy - - - - - - - Johan den Dunnen 00216934
0000165386 - cardiomyopathy - - - - - - - Johan den Dunnen 00216935
0000165387 - cardiomyopathy - - - - - - - Johan den Dunnen 00216936
0000165388 - cardiomyopathy - - - - - - - Johan den Dunnen 00216937
0000165389 - cardiomyopathy - - - - - - - Johan den Dunnen 00216938
0000165390 - cardiomyopathy - - - - - - - Johan den Dunnen 00216939
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