gene_id
stringlengths 1
9
| symbol
stringclasses 1
value | concept_id
stringlengths 3
208
| concept_name
stringlengths 4
405
⌀ | concept_origin
stringclasses 5
values | url
stringlengths 3
48
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|---|---|---|---|---|---|
6927 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
208 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
6928 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3667 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
10644 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
8660 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
2645 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3990 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
5078 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
6934 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3159 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
4760 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
56729 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
5468 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3172 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
7466 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
5167 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3569 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
6833 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
6514 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3767 | nan | 125853 | TYPE 2 DIABETES MELLITUS | OMIM MedGen | https://omim.org/entry/125853 |
3123 | nan | 126200 | MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | OMIM MedGen | https://omim.org/entry/126200 |
5133 | nan | 126200 | MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | OMIM MedGen | https://omim.org/entry/126200 |
3119 | nan | 126200 | MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | OMIM MedGen | https://omim.org/entry/126200 |
166929 | nan | 126550 | CALVARIAL DOUGHNUT LESIONS WITH BONE FRAGILITY | OMIM MedGen | https://omim.org/entry/126550 |
2202 | nan | 126600 | DOYNE HONEYCOMB RETINAL DYSTROPHY | OMIM MedGen | https://omim.org/entry/126600 |
3075 | nan | 126700 | BASAL LAMINAR DRUSEN | OMIM MedGen | https://omim.org/entry/126700 |
63901 | nan | 127000 | KENNY-CAFFEY SYNDROME, TYPE 2 | OMIM MedGen | https://omim.org/entry/127000 |
6473 | nan | 127300 | LERI-WEILL DYSCHONDROSTEOSIS | OMIM MedGen | https://omim.org/entry/127300 |
103 | nan | 127400 | DYSCHROMATOSIS SYMMETRICA HEREDITARIA | OMIM MedGen | https://omim.org/entry/127400 |
23328 | nan | 127500 | DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1 | OMIM MedGen | https://omim.org/entry/127500 |
7012 | nan | 127550 | DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1 | OMIM MedGen | https://omim.org/entry/127550 |
26277 | nan | 127550 | DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1 | OMIM MedGen | https://omim.org/entry/127550 |
7015 | nan | 127550 | DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 1 | OMIM MedGen | https://omim.org/entry/127550 |
161582 | nan | 127700 | DYSLEXIA, SUSCEPTIBILITY TO, 1 | OMIM MedGen | https://omim.org/entry/127700 |
2629 | nan | 127750 | DEMENTIA, LEWY BODY | OMIM MedGen | https://omim.org/entry/127750 |
6620 | nan | 127750 | DEMENTIA, LEWY BODY | OMIM MedGen | https://omim.org/entry/127750 |
6622 | nan | 127750 | DEMENTIA, LEWY BODY | OMIM MedGen | https://omim.org/entry/127750 |
1861 | nan | 128100 | DYSTONIA 1, TORSION, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/128100 |
10382 | nan | 128101 | DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/128101 |
112476 | nan | 128200 | EPISODIC KINESIGENIC DYSKINESIA 1 | OMIM MedGen | https://omim.org/entry/128200 |
2643 | nan | 128230 | DYSTONIA, DOPA-RESPONSIVE | OMIM MedGen | https://omim.org/entry/128230 |
478 | nan | 128235 | DYSTONIA 12 | OMIM MedGen | https://omim.org/entry/128235 |
56916 | nan | 129200 | BASAN SYNDROME | OMIM MedGen | https://omim.org/entry/129200 |
8626 | nan | 129400 | RAPP-HODGKIN SYNDROME | OMIM MedGen | https://omim.org/entry/129400 |
10913 | nan | 129490 | ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/129490 |
128178 | nan | 129490 | ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/129490 |
10804 | nan | 129500 | CLOUSTON SYNDROME | OMIM MedGen | https://omim.org/entry/129500 |
2200 | nan | 129600 | ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/129600 |
1289 | nan | 130000 | EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 1 | OMIM MedGen | https://omim.org/entry/130000 |
1290 | nan | 130010 | EHLERS-DANLOS SYNDROME, CLASSIC TYPE, 2 | OMIM MedGen | https://omim.org/entry/130010 |
1281 | nan | 130050 | EHLERS-DANLOS SYNDROME, VASCULAR TYPE | OMIM MedGen | https://omim.org/entry/130050 |
1277 | nan | 130060 | EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 | OMIM MedGen | https://omim.org/entry/130060 |
11285 | nan | 130070 | EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1 | OMIM MedGen | https://omim.org/entry/130070 |
715 | nan | 130080 | EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 1 | OMIM MedGen | https://omim.org/entry/130080 |
6708 | nan | 130600 | ELLIPTOCYTOSIS 2 | OMIM MedGen | https://omim.org/entry/130600 |
1028 | nan | 130650 | BECKWITH-WIEDEMANN SYNDROME | OMIM MedGen | https://omim.org/entry/130650 |
10984 | nan | 130650 | BECKWITH-WIEDEMANN SYNDROME | OMIM MedGen | https://omim.org/entry/130650 |
3784 | nan | 130650 | BECKWITH-WIEDEMANN SYNDROME | OMIM MedGen | https://omim.org/entry/130650 |
105259599 | nan | 130650 | BECKWITH-WIEDEMANN SYNDROME | OMIM MedGen | https://omim.org/entry/130650 |
3481 | nan | 130650 | BECKWITH-WIEDEMANN SYNDROME | OMIM MedGen | https://omim.org/entry/130650 |
4854 | nan | 130720 | LATERAL MENINGOCELE SYNDROME | OMIM MedGen | https://omim.org/entry/130720 |
286077 | nan | 130900 | AMELOGENESIS IMPERFECTA, TYPE IIIA | OMIM MedGen | https://omim.org/entry/130900 |
4221 | nan | 131100 | MULTIPLE ENDOCRINE NEOPLASIA, TYPE I | OMIM MedGen | https://omim.org/entry/131100 |
7040 | nan | 131300 | CAMURATI-ENGELMANN DISEASE | OMIM MedGen | https://omim.org/entry/131300 |
5159 | nan | 131440 | MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA | OMIM MedGen | https://omim.org/entry/131440 |
1294 | nan | 131705 | TRANSIENT BULLOUS DERMOLYSIS OF THE NEWBORN | OMIM MedGen | https://omim.org/entry/131705 |
1294 | nan | 131750 | EPIDERMOLYSIS BULLOSA DYSTROPHICA, AUTOSOMAL DOMINANT | OMIM MedGen | https://omim.org/entry/131750 |
3861 | nan | 131760 | EPIDERMOLYSIS BULLOSA SIMPLEX 1A, GENERALIZED SEVERE | OMIM MedGen | https://omim.org/entry/131760 |
3852 | nan | 131760 | EPIDERMOLYSIS BULLOSA SIMPLEX 1A, GENERALIZED SEVERE | OMIM MedGen | https://omim.org/entry/131760 |
3861 | nan | 131800 | EPIDERMOLYSIS BULLOSA SIMPLEX 1C, LOCALIZED | OMIM MedGen | https://omim.org/entry/131800 |
1294 | nan | 131850 | EPIDERMOLYSIS BULLOSA DYSTROPHICA, PRETIBIAL | OMIM MedGen | https://omim.org/entry/131850 |
3861 | nan | 131900 | EPIDERMOLYSIS BULLOSA SIMPLEX 1B, GENERALIZED INTERMEDIATE | OMIM MedGen | https://omim.org/entry/131900 |
5339 | nan | 131950 | EPIDERMOLYSIS BULLOSA SIMPLEX 5A, OGNA TYPE | OMIM MedGen | https://omim.org/entry/131950 |
3852 | nan | 131960 | EPIDERMOLYSIS BULLOSA SIMPLEX 2F, WITH MOTTLED PIGMENTATION | OMIM MedGen | https://omim.org/entry/131960 |
1294 | nan | 132000 | EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS | OMIM MedGen | https://omim.org/entry/132000 |
1311 | nan | 132400 | EPIPHYSEAL DYSPLASIA, MULTIPLE, 1 | OMIM MedGen | https://omim.org/entry/132400 |
1280 | nan | 132450 | EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH MYOPIA AND CONDUCTIVE DEAFNESS | OMIM MedGen | https://omim.org/entry/132450 |
1499 | nan | 132600 | PILOMATRIXOMA | OMIM MedGen | https://omim.org/entry/132600 |
1540 | nan | 132700 | CYLINDROMATOSIS, FAMILIAL | OMIM MedGen | https://omim.org/entry/132700 |
7046 | nan | 132800 | MULTIPLE SELF-HEALING SQUAMOUS EPITHELIOMA, SUSCEPTIBILITY TO | OMIM MedGen | https://omim.org/entry/132800 |
4629 | nan | 132900 | AORTIC ANEURYSM, FAMILIAL THORACIC 4 | OMIM MedGen | https://omim.org/entry/132900 |
6335 | nan | 133020 | ERYTHERMALGIA, PRIMARY | OMIM MedGen | https://omim.org/entry/133020 |
10019 | nan | 133100 | ERYTHROCYTOSIS, FAMILIAL, 1 | OMIM MedGen | https://omim.org/entry/133100 |
3717 | nan | 133100 | ERYTHROCYTOSIS, FAMILIAL, 1 | OMIM MedGen | https://omim.org/entry/133100 |
2057 | nan | 133100 | ERYTHROCYTOSIS, FAMILIAL, 1 | OMIM MedGen | https://omim.org/entry/133100 |
2065 | nan | 133180 | ERYTHROLEUKEMIA, FAMILIAL, SUSCEPTIBILITY TO | OMIM MedGen | https://omim.org/entry/133180 |
6785 | nan | 133190 | SPINOCEREBELLAR ATAXIA 34 | OMIM MedGen | https://omim.org/entry/133190 |
2707 | nan | 133200 | ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 1 | OMIM MedGen | https://omim.org/entry/133200 |
6049 | nan | 133239 | ESOPHAGEAL CANCER | OMIM MedGen | https://omim.org/entry/133239 |
7048 | nan | 133239 | ESOPHAGEAL CANCER | OMIM MedGen | https://omim.org/entry/133239 |
11178 | nan | 133239 | ESOPHAGEAL CANCER | OMIM MedGen | https://omim.org/entry/133239 |
51741 | nan | 133239 | ESOPHAGEAL CANCER | OMIM MedGen | https://omim.org/entry/133239 |
1630 | nan | 133239 | ESOPHAGEAL CANCER | OMIM MedGen | https://omim.org/entry/133239 |
2074 | nan | 133540 | COCKAYNE SYNDROME B | OMIM MedGen | https://omim.org/entry/133540 |
2131 | nan | 133700 | EXOSTOSES, MULTIPLE, TYPE I | OMIM MedGen | https://omim.org/entry/133700 |
2132 | nan | 133701 | EXOSTOSES, MULTIPLE, TYPE II | OMIM MedGen | https://omim.org/entry/133701 |
8322 | nan | 133780 | EXUDATIVE VITREORETINOPATHY 1 | OMIM MedGen | https://omim.org/entry/133780 |
4041 | nan | 133780 | EXUDATIVE VITREORETINOPATHY 1 | OMIM MedGen | https://omim.org/entry/133780 |
2628 | nan | 134600 | FANCONI RENOTUBULAR SYNDROME 1 | OMIM MedGen | https://omim.org/entry/134600 |
Subsets and Splits