Source: CURATED ×
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		35 0 1 3.4E-03 0 0
CUI: C0087012
Disease: Ataxia, Spinocerebellar
Ataxia, Spinocerebellar 		34 0 1 3.4E-03 0 0
CUI: C0752120
Disease: Spinocerebellar Ataxia Type 1
Spinocerebellar Ataxia Type 1 		34 0 1 3.4E-03 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		34 0 1 3.4E-03 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		34 0 1 3.4E-03 0 0
CUI: C0752124
Disease: Spinocerebellar Ataxia Type 6 (disorder)
Spinocerebellar Ataxia Type 6 (disorder) 		34 0 1 3.4E-03 0 0
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		34 0 1 3.4E-03 0 0
CUI: C0263454
Disease: Chloracne
Chloracne 		33 0 1 3.4E-03 0 0
CUI: C0029925
Disease: Ovarian Carcinoma
Ovarian Carcinoma 		30 0 1 3.5E-03 0 0
CUI: C0496920
Disease: Neoplasm of uncertain or unknown behavior of ovary
Neoplasm of uncertain or unknown behavior of ovary 		29 0 1 3.5E-03 0 0
CUI: C2713368
Disease: Hematopoetic Myelodysplasia
Hematopoetic Myelodysplasia 		29 0 1 3.5E-03 0 0
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2 		29 0 1 3.5E-03 0 0
CUI: C0086432
Disease: Hyalinosis, Segmental Glomerular
Hyalinosis, Segmental Glomerular 		28 0 1 3.5E-03 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		27 0 1 3.5E-03 0 0
CUI: C0030312
Disease: Pancytopenia
Pancytopenia 		26 0 1 3.5E-03 0 0
CUI: C0011053
Disease: Deafness
Deafness 		25 0 1 3.5E-03 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		25 0 1 3.5E-03 0 0
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		25 0 1 3.5E-03 0 0
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		25 0 1 3.5E-03 0 0
CUI: C0028326
Disease: Noonan Syndrome
Noonan Syndrome 		24 0 1 3.5E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		24 0 1 3.5E-03 0 0
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		23 0 1 3.6E-03 0 0
CUI: C1708353
Disease: Hereditary Paraganglioma-Pheochromocytoma Syndrome
Hereditary Paraganglioma-Pheochromocytoma Syndrome 		23 0 1 3.6E-03 0 0
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis 		22 0 1 3.6E-03 0 0
CUI: C0018781
Disease: Noise-induced hearing loss
Noise-induced hearing loss 		22 0 1 3.6E-03 0 0