Source: ALL
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: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 4 9.5E-02 0 0
CUI: C0272183
Disease: Qualitative abnormality of granulocyte
Qualitative abnormality of granulocyte 		22 0 4 8.7E-02 0 0
CUI: C0858681
Disease: Vitiligo vulgaris
Vitiligo vulgaris 		13 0 3 7.9E-02 0 0
CUI: C4087347
Disease: Autosomal dominant cerebellar ataxia
Autosomal dominant cerebellar ataxia 		31 0 4 7.3E-02 0 0
CUI: C1335354
Disease: Parotid Gland Adenocarcinoma
Parotid Gland Adenocarcinoma 		2 0 2 7.1E-02 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		17 0 3 7.1E-02 0 0
CUI: C3825858
Disease: Pediatric respiratory diseases
Pediatric respiratory diseases 		2 0 2 7.1E-02 0 0
CUI: C1850383
Disease: Neuropathy, Painful
Neuropathy, Painful 		18 0 3 7.0E-02 0 0
CUI: C0393578
Disease: Pallidoluysian degeneration
Pallidoluysian degeneration 		3 0 2 6.9E-02 0 0
CUI: C0745674
Disease: Dilated left ventricle
Dilated left ventricle 		3 0 2 6.9E-02 0 0
CUI: C0019156
Disease: Hepatic Veno-Occlusive Disease
Hepatic Veno-Occlusive Disease 		37 0 4 6.6E-02 0 0
CUI: C4014261
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 16 		5 0 2 6.5E-02 0 0
CUI: C0239849
Disease: Harlequin Fetus
Harlequin Fetus 		73 0 6 6.3E-02 0 0
CUI: C0037061
Disease: Siderosis
Siderosis 		23 0 3 6.2E-02 0 0
CUI: C0037997
Disease: Splenic Diseases
Splenic Diseases 		6 0 2 6.2E-02 0 0
CUI: C0392622
Disease: Toxic effect of carbon tetrachloride
Toxic effect of carbon tetrachloride 		6 0 2 6.2E-02 0 0
CUI: C0730281
Disease: Proliferative diabetic retinopathy - quiescent
Proliferative diabetic retinopathy - quiescent 		6 0 2 6.2E-02 0 0
CUI: C1336840
Disease: Papillary renal cell carcinoma type 2
Papillary renal cell carcinoma type 2 		6 0 2 6.2E-02 0 0
CUI: C1695782
Disease: Cerebral hypoperfusion
Cerebral hypoperfusion 		40 0 4 6.2E-02 0 0
CUI: C3273225
Disease: Hereditary Neurodegenerative Disorder
Hereditary Neurodegenerative Disorder 		6 0 2 6.2E-02 0 0
CUI: C3711380
Disease: Huntington Disease-Like Syndrome
Huntington Disease-Like Syndrome 		6 0 2 6.2E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 6 6.1E-02 0 0
CUI: C0008439
Disease: Chondritis
Chondritis 		7 0 2 6.1E-02 0 0
CUI: C0031306
Disease: Phagocyte Bactericidal Dysfunction
Phagocyte Bactericidal Dysfunction 		7 0 2 6.1E-02 0 0
CUI: C0149904
Disease: Cholestatic hepatitis
Cholestatic hepatitis 		7 0 2 6.1E-02 0 0