Disease_1
stringlengths 4
61
| Disease_2
stringlengths 4
61
| Similarity_Score
stringclasses 78
values |
|---|---|---|
Congenital Abnormalities | Hermanski-Pudlak Syndrome | 0.22612546428933034 |
Congenital Abnormalities | XX 46 Gonadal Dysgenesis | 0.3430264696222015 |
Familial Hypertrophic Cardiomyopathy | Congenital Abnormalities | 0.27212855635537503 |
Chromosome Disorders | Congenital Abnormalities | 0.5180525369110661 |
Congenital Abnormalities | Sex Chromosome Disorders | 0.4373356273919856 |
Inherited Blood Coagulation Disorders | Congenital Abnormalities | 0.27212855635537503 |
Congenital Abnormalities | Septo-Optic Dysplasia | 0.38355214601147614 |
Familial Amyloidosis | Congenital Abnormalities | 0.22612546428933034 |
Familial Amyloid Neuropathies | Congenital Abnormalities | 0.22612546428933034 |
Familial Cerebral Amyloid Angiopathy | Congenital Abnormalities | 0.18766904849475052 |
Biotinidase Deficiency | Congenital Abnormalities | 0.15364182357778045 |
Congenital Abnormalities | Holocarboxylase Synthetase Deficiency | 0.15364182357778045 |
Congenital Abnormalities | Autosomal Dominant Optic Atrophy | 0.18766904849475052 |
Congenital Abnormalities | Leber Hereditary Optic Atrophy | 0.18766904849475052 |
Congenital Abnormalities | Sialic Acid Storage Disease | 0.15364182357778045 |
Congenital Hypoplastic Anemia | Congenital Abnormalities | 0.27212855635537503 |
Diamond-Blackfan Anemia | Congenital Abnormalities | 0.22612546428933034 |
Congenital Abnormalities | Jervell-Lange Nielsen Syndrome | 0.3430264696222015 |
Congenital Abnormalities | Romano-Ward Syndrome | 0.3430264696222015 |
Congenital Abnormalities | Denys-Drash Syndrome | 0.3430264696222015 |
Congenital Abnormalities | Inborn Genetic Diseases | 0.3324584892504371 |
Congenital Abnormalities | Cytochrome-c Oxidase Deficiency | 0.22612546428933034 |
Congenital Abnormalities | Hajdu-Cheney Syndrome | 0.4373356273919856 |
Congenital Abnormalities | Congenital Lower Extremity Deformities | 0.38355214601147614 |
Congenital Abnormalities | Congenital Upper Extremity Deformities | 0.38355214601147614 |
Alexander Disease | Congenital Abnormalities | 0.22612546428933034 |
Congenital Abnormalities | X-Linked Mental Retardation | 0.22612546428933034 |
Coffin-Lowry Syndrome | Congenital Abnormalities | 0.18766904849475052 |
Congenital Abnormalities | Oculopharyngeal Muscular Dystrophy | 0.22612546428933034 |
Congenital Abnormalities | X-Linked Genetic Diseases | 0.27212855635537503 |
Congenital Abnormalities | Inborn Errors Steroid Metabolism | 0.22612546428933034 |
Congenital Abnormalities | Apparent Mineralocorticoid Excess Syndrome | 0.18766904849475052 |
Congenital Abnormalities | Lymphatic Abnormalities | 0.5180525369110661 |
Congenital Abnormalities | LEOPARD Syndrome | 0.4373356273919856 |
Congenital Abnormalities | Congenital Hyperinsulinism | 0.27212855635537503 |
Congenital Abnormalities | Mannosidase Deficiency Diseases | 0.18766904849475052 |
Congenital Abnormalities | beta-Mannosidosis | 0.15364182357778045 |
Congenital Abnormalities | Laron Syndrome | 0.22612546428933034 |
Congenital Abnormalities | Lingual Thyroid | 0.4373356273919856 |
Congenital Abnormalities | Hereditary Coproporphyria | 0.18766904849475052 |
Congenital Abnormalities | Variegate Porphyria | 0.18766904849475052 |
Congenital Abnormalities | Erythropoietic Protoporphyria | 0.18766904849475052 |
CADASIL | Congenital Abnormalities | 0.27212855635537503 |
Congenital Abnormalities | Nesidioblastosis | 0.22612546428933034 |
Congenital Abnormalities | Lingual Goiter | 0.38355214601147614 |
Adrenogenital Syndrome | Congenital Abnormalities | 0.38355214601147614 |
Congenital Abnormalities | Nonsynostotic Plagiocephaly | 0.3430264696222015 |
Congenital Abnormalities | Limb-Girdle Muscular Dystrophies | 0.22612546428933034 |
Congenital Abnormalities | AB Variant Tay-Sachs Disease | 0.06323372317637754 |
Congenital Abnormalities | Distal Myopathies | 0.22612546428933034 |
Congenital Abnormalities | Graves Ophthalmopathy | 0.22612546428933034 |
Congenital Abnormalities | Familial Dysalbuminemic Hyperthyroxinemia | 0.27212855635537503 |
Andersen Syndrome | Congenital Abnormalities | 0.3430264696222015 |
Congenital Abnormalities | Thyroid Dysgenesis | 0.5180525369110661 |
Congenital Abnormalities | Sexual Infantilism | 0.3430264696222015 |
Congenital Abnormalities | Ovotesticular Disorders of Sex Development | 0.38355214601147614 |
Congenital Abnormalities | Y-Linked Genetic Diseases | 0.27212855635537503 |
Congenital Abnormalities | Mulibrey Nanism | 0.22612546428933034 |
Congenital Abnormalities | Neonatal Hyperbilirubinemia | 0.27212855635537503 |
Congenital Abnormalities | Glycogen Storage Disease Type IIb | 0.22612546428933034 |
Congenital Abnormalities | Frasier Syndrome | 0.3430264696222015 |
Congenital Abnormalities | Usher Syndromes | 0.38355214601147614 |
Congenital Abnormalities | Hypoalphalipoproteinemias | 0.15364182357778045 |
Congenital Abnormalities | Familial Partial Lipodystrophy | 0.22612546428933034 |
Congenital Abnormalities | Congenital Generalized Lipodystrophy | 0.18766904849475052 |
Congenital Abnormalities | Sulfatidosis | 0.12229063423583264 |
Congenital Abnormalities | Multiple Sulfatase Deficiency Disease | 0.09245500931811057 |
Congenital Abnormalities | Type A Niemann-Pick Disease | 0.09245500931811057 |
Congenital Abnormalities | Type B Niemann-Pick Disease | 0.09245500931811057 |
Congenital Abnormalities | Type C Niemann-Pick Disease | 0.09245500931811057 |
Congenital Abnormalities | Infantile Refsum Disease | 0.18766904849475052 |
Congenital Abnormalities | Familial Hypophosphatemic Rickets | 0.18766904849475052 |
Congenital Abnormalities | Hyper-IgM Immunodeficiency Syndrome | 0.27212855635537503 |
Congenital Abnormalities | Type 1 Hyper-IgM Immunodeficiency Syndrome | 0.22612546428933034 |
Congenital Abnormalities | Anhidrotic Ectodermal Dysplasia 1 | 0.38355214601147614 |
Congenital Abnormalities | Anhidrotic Ectodermal Dysplasia 3 | 0.38355214601147614 |
Congenital Abnormalities | Autosomal Recessive Hypohidrotic Ectodermal Dysplasia | 0.38355214601147614 |
Congenital Abnormalities | Hereditary Mucosal Leukokeratosis | 0.22612546428933034 |
Congenital Abnormalities | Epidermolytic Palmoplantar Keratoderma | 0.15364182357778045 |
Congenital Abnormalities | Pachyonychia Congenita | 0.38355214601147614 |
Congenital Abnormalities | Juvenile Epithelial of Meesmann Corneal Dystrophy | 0.18766904849475052 |
Congenital Abnormalities | Ichthyosis Bullosa of Siemens | 0.38355214601147614 |
Congenital Abnormalities | Gitelman Syndrome | 0.22612546428933034 |
Congenital Abnormalities | Nuchal Cord | 0.27212855635537503 |
Congenital Abnormalities | X-Linked Combined Immunodeficiency Diseases | 0.22612546428933034 |
Brugada Syndrome | Congenital Abnormalities | 0.27212855635537503 |
Congenital Abnormalities | Sebaceous of Jadassohn Nevus | 0.4373356273919856 |
Congenital Abnormalities | Deaf-Blind Disorders | 0.4373356273919856 |
Congenital Abnormalities | Dihydropyrimidine Dehydrogenase Deficiency | 0.18766904849475052 |
Congenital Abnormalities | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | 0.18766904849475052 |
Congenital Abnormalities | Mevalonate Kinase Deficiency | 0.22612546428933034 |
Congenital Abnormalities | Vascular Malformations | 0.4373356273919856 |
Congenital Abnormalities | Vein of Galen Malformations | 0.3430264696222015 |
Congenital Abnormalities | Group II Malformations of Cortical Development | 0.38355214601147614 |
Congenital Abnormalities | Lissencephaly | 0.3430264696222015 |
Congenital Abnormalities | Ectopia Cordis | 0.38355214601147614 |
Congenital Abnormalities | Myocardial Bridging | 0.3430264696222015 |
Congenital Abnormalities | Periventricular Nodular Heterotopia | 0.3430264696222015 |
Congenital Abnormalities | Patent Foramen Ovale | 0.310198271667516 |
Congenital Abnormalities | Neonatal Alloimmune Thrombocytopenia | 0.27212855635537503 |
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