rank int64 1 16 | score float64 0.58 1 | disease_name stringlengths 4 127 | disease_identifier stringlengths 7 12 |
|---|---|---|---|
13 | 0.8008 | Arrhythmogenic right ventricular dysplasia 10 | OMIM:610193 |
14 | 0.7999 | X-linked Emery-Dreifuss muscular dystrophy | ORPHA:98863 |
15 | 0.7996 | Cockayne syndrome, type A | OMIM:216400 |
16 | 0.797 | Heart-hand syndrome, Slovenian type | ORPHA:168796 |
1 | 0.8706 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
2 | 0.8607 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
3 | 0.8431 | Sick sinus syndrome 2 | OMIM:163800 |
4 | 0.8398 | Cardiomyopathy, dilated, 1D | OMIM:601494 |
5 | 0.8329 | Cardiomyopathy, hypertrophic 6 | OMIM:600858 |
6 | 0.8308 | ?Sick sinus syndrome 4 | OMIM:619464 |
7 | 0.8306 | Atrial fibrillation, familial, 7 | OMIM:612240 |
8 | 0.8303 | Long QT syndrome 4 | OMIM:600919 |
9 | 0.8298 | Long QT syndrome 15 | OMIM:616249 |
10 | 0.8143 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
11 | 0.8139 | Long QT syndrome 8 | OMIM:618447 |
12 | 0.8086 | Romano-Ward syndrome | ORPHA:101016 |
13 | 0.8061 | Long QT syndrome 5 | OMIM:613695 |
14 | 0.8027 | Cockayne syndrome, type B | OMIM:133540 |
15 | 0.7952 | Sick sinus syndrome 1 | OMIM:608567 |
16 | 0.7913 | Long QT syndrome 9 | OMIM:611818 |
1 | 0.8467 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.828 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
3 | 0.8274 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
4 | 0.826 | Cockayne syndrome, type B | OMIM:133540 |
5 | 0.8216 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
6 | 0.8182 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
7 | 0.8157 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
8 | 0.8123 | McLeod syndrome | OMIM:300842 |
9 | 0.8101 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
10 | 0.8096 | Cardiomyopathy, dilated, 1E | OMIM:601154 |
11 | 0.8082 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
12 | 0.8078 | Marfan lipodystrophy syndrome | OMIM:616914 |
13 | 0.8008 | Arrhythmogenic right ventricular dysplasia 10 | OMIM:610193 |
14 | 0.7999 | X-linked Emery-Dreifuss muscular dystrophy | ORPHA:98863 |
15 | 0.7996 | Cockayne syndrome, type A | OMIM:216400 |
16 | 0.797 | Heart-hand syndrome, Slovenian type | ORPHA:168796 |
1 | 0.8549 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8392 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
3 | 0.8353 | Cockayne syndrome, type B | OMIM:133540 |
4 | 0.8311 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
5 | 0.8286 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
6 | 0.8211 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
7 | 0.8201 | Marfan lipodystrophy syndrome | OMIM:616914 |
8 | 0.8199 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
9 | 0.8183 | Heart-hand syndrome, Slovenian type | ORPHA:168796 |
10 | 0.817 | Cardiomyopathy, dilated, 1E | OMIM:601154 |
11 | 0.8169 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
12 | 0.8109 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
13 | 0.8109 | Desminopathy | ORPHA:98909 |
14 | 0.8093 | X-linked Emery-Dreifuss muscular dystrophy | ORPHA:98863 |
15 | 0.8052 | Brugada syndrome 1 | OMIM:601144 |
16 | 0.8039 | Cardiomyopathy, hypertrophic, 23, with or without LVNC | OMIM:612158 |
1 | 0.8549 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8392 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
3 | 0.8353 | Cockayne syndrome, type B | OMIM:133540 |
4 | 0.8311 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
5 | 0.8286 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
6 | 0.8211 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
7 | 0.8201 | Marfan lipodystrophy syndrome | OMIM:616914 |
8 | 0.8199 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
9 | 0.8183 | Heart-hand syndrome, Slovenian type | ORPHA:168796 |
10 | 0.817 | Cardiomyopathy, dilated, 1E | OMIM:601154 |
11 | 0.8169 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
12 | 0.8109 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
13 | 0.8109 | Desminopathy | ORPHA:98909 |
14 | 0.8093 | X-linked Emery-Dreifuss muscular dystrophy | ORPHA:98863 |
15 | 0.8052 | Brugada syndrome 1 | OMIM:601144 |
16 | 0.8039 | Cardiomyopathy, hypertrophic, 23, with or without LVNC | OMIM:612158 |
1 | 0.8641 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8508 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
3 | 0.8484 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
4 | 0.8411 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
5 | 0.8246 | Cockayne syndrome, type B | OMIM:133540 |
6 | 0.8209 | Desminopathy | ORPHA:98909 |
7 | 0.8167 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
8 | 0.8153 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
9 | 0.8147 | Cardiomyopathy, dilated, 1G | OMIM:604145 |
10 | 0.8147 | Cardiomyopathy, dilated, 1D | OMIM:601494 |
11 | 0.8117 | Naxos disease | OMIM:601214 |
12 | 0.8117 | Cardiomyopathy, hypertrophic 6 | OMIM:600858 |
13 | 0.8113 | Cardiomyopathy, dilated, 1L | OMIM:606685 |
14 | 0.8094 | Cardiomyopathy, familial hypertrophic, 26 | OMIM:617047 |
15 | 0.8093 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
16 | 0.8093 | Proteasome-associated autoinflammatory syndrome 1 and digenic forms | OMIM:256040 |
1 | 0.8472 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8353 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
3 | 0.8285 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
4 | 0.8234 | Cockayne syndrome, type B | OMIM:133540 |
5 | 0.8179 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
6 | 0.8151 | Cardiomyopathy, dilated, 1D | OMIM:601494 |
7 | 0.812 | Cardiomyopathy, dilated, 1L | OMIM:606685 |
8 | 0.8114 | Marfan lipodystrophy syndrome | OMIM:616914 |
9 | 0.809 | Proteasome-associated autoinflammatory syndrome 1 and digenic forms | OMIM:256040 |
10 | 0.8089 | McLeod syndrome | OMIM:300842 |
11 | 0.8041 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
12 | 0.804 | Naxos disease | OMIM:601214 |
13 | 0.7982 | Cockayne syndrome, type A | OMIM:216400 |
14 | 0.7975 | Desminopathy | ORPHA:98909 |
15 | 0.7969 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
16 | 0.7966 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
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