rank int64 1 16 | score float64 0.58 1 | disease_name stringlengths 4 127 | disease_identifier stringlengths 7 12 |
|---|---|---|---|
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 | 0.874 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8616 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
3 | 0.8521 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
4 | 0.843 | Desminopathy | ORPHA:98909 |
5 | 0.8378 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
6 | 0.834 | Cockayne syndrome, type B | OMIM:133540 |
7 | 0.8324 | Cardiomyopathy, dilated, 1G | OMIM:604145 |
8 | 0.8278 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
9 | 0.8198 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
10 | 0.8196 | Cardiomyopathy, hypertrophic 6 | OMIM:600858 |
11 | 0.8194 | Cardiomyopathy, familial hypertrophic, 26 | OMIM:617047 |
12 | 0.8188 | Marfan lipodystrophy syndrome | OMIM:616914 |
13 | 0.8184 | Naxos disease | OMIM:601214 |
14 | 0.8182 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
15 | 0.8175 | Cardiomyopathy, dilated, 1E | OMIM:601154 |
16 | 0.8174 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
1 | 0.8276 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.8246 | Cockayne syndrome, type B | OMIM:133540 |
3 | 0.8152 | McLeod syndrome | OMIM:300842 |
4 | 0.8132 | Marfan lipodystrophy syndrome | OMIM:616914 |
5 | 0.8093 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
6 | 0.8067 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
7 | 0.8038 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
8 | 0.8 | Mandibuloacral dysplasia with type B lipodystrophy | ORPHA:90154 |
9 | 0.7973 | Cockayne syndrome, type A | OMIM:216400 |
10 | 0.7972 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
11 | 0.7971 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
12 | 0.7944 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
13 | 0.7936 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
14 | 0.7914 | Lipodystrophy, familial partial, type 7 | OMIM:606721 |
15 | 0.7908 | Proteasome-associated autoinflammatory syndrome 1 and digenic forms | OMIM:256040 |
16 | 0.7907 | Cardiomyopathy, dilated, 1D | OMIM:601494 |
1 | 0.8712 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
2 | 0.8422 | Danon disease | OMIM:300257 |
3 | 0.8044 | Long QT syndrome 15 | OMIM:616249 |
4 | 0.8024 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
5 | 0.795 | Atrial standstill | ORPHA:1344 |
6 | 0.791 | Muscular dystrophy, limb-girdle, autosomal recessive 25 | OMIM:616812 |
7 | 0.7904 | ?Cardiomyopathy, dilated, 1OO | OMIM:620247 |
8 | 0.7888 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
9 | 0.7821 | Cockayne syndrome, type B | OMIM:133540 |
10 | 0.7805 | Long QT syndrome 14 | OMIM:616247 |
11 | 0.7803 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
12 | 0.7786 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
13 | 0.7727 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
14 | 0.7717 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
15 | 0.7709 | McLeod syndrome | OMIM:300842 |
16 | 0.7699 | Autosomal recessive Emery-Dreifuss muscular dystrophy | ORPHA:98855 |
1 | 0.8564 | Cardiomyopathy, familial hypertrophic, 26 | OMIM:617047 |
2 | 0.8521 | ?Atrial fibrillation 15 | OMIM:615770 |
3 | 0.846 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
4 | 0.8301 | ?Cardiomyopathy, familial hypertrophic, 30, atrial | OMIM:620734 |
5 | 0.8243 | Myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy | OMIM:619424 |
6 | 0.8238 | Cardiomyopathy, hypertrophic, 8 | OMIM:608751 |
7 | 0.8214 | Cardiomyopathy, familial hypertrophic, 28 | OMIM:619402 |
8 | 0.8168 | Cardiomyopathy, familial restrictive, 1 | OMIM:115210 |
9 | 0.8154 | Chronic atrial and intestinal dysrhythmia | OMIM:616201 |
10 | 0.8132 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
11 | 0.8113 | Cardiomyopathy, dilated, 2G | OMIM:619897 |
12 | 0.806 | Atrial fibrillation, familial, 10 | OMIM:614022 |
13 | 0.803 | Familial isolated restrictive cardiomyopathy | ORPHA:75249 |
14 | 0.7959 | Marfan lipodystrophy syndrome | OMIM:616914 |
15 | 0.7938 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
16 | 0.7924 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
1 | 0.8478 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | ORPHA:300751 |
2 | 0.829 | Cardiac conduction disease with or without dilated cardiomyopathy | OMIM:616117 |
3 | 0.8189 | Cockayne syndrome, type B | OMIM:133540 |
4 | 0.8184 | Cardiomyopathy, dilated, 1A | OMIM:115200 |
5 | 0.8118 | Marfan lipodystrophy syndrome | OMIM:616914 |
6 | 0.8074 | Lipodystrophy, familial partial, type 7 | OMIM:606721 |
7 | 0.8044 | Naxos disease | OMIM:601214 |
8 | 0.8034 | Desminopathy | ORPHA:98909 |
9 | 0.8032 | Congenital myopathy 5 with cardiomyopathy | OMIM:611705 |
10 | 0.7991 | Proteasome-associated autoinflammatory syndrome 1 and digenic forms | OMIM:256040 |
11 | 0.7984 | Mandibuloacral dysplasia with type B lipodystrophy | OMIM:608612 |
12 | 0.7971 | Ventricular tachycardia, catecholaminergic polymorphic, 1 | OMIM:604772 |
13 | 0.7967 | Autosomal dominant Emery-Dreifuss muscular dystrophy | ORPHA:98853 |
14 | 0.7958 | Nestor-Guillermo progeria syndrome | OMIM:614008 |
15 | 0.7957 | Cardiomyopathy, dilated, 1D | OMIM:601494 |
16 | 0.795 | Cutis laxa, autosomal dominant | OMIM:123700 |
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 |
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