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: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 1 1.8E-03 0 0
CUI: C0029227
Disease: Delirium, Dementia, Amnestic, Cognitive Disorders
Delirium, Dementia, Amnestic, Cognitive Disorders 		83 0 1 1.2E-02 0 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		2872 0 1 3.5E-04 0 0
CUI: C0037763
Disease: Spasm
Spasm 		172 0 1 5.8E-03 0 0
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		1658 0 1 6.0E-04 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 4.7E-03 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases 		130 0 1 7.6E-03 0 0
CUI: C0085543
Disease: Epilepsia Partialis Continua
Epilepsia Partialis Continua 		15 0 1 6.2E-02 0 0
CUI: C0153676
Disease: Secondary malignant neoplasm of lung
Secondary malignant neoplasm of lung 		1370 0 2 1.5E-03 0 0
CUI: C0178874
Disease: Tumor Progression
Tumor Progression 		3865 0 1 2.6E-04 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 1 3.7E-02 0 0
CUI: C0206698
Disease: Cholangiocarcinoma
Cholangiocarcinoma 		877 0 1 1.1E-03 0 0
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma 		1377 0 1 7.3E-04 0 0
CUI: C0220668
Disease: Congenital contractural arachnodactyly
Congenital contractural arachnodactyly 		559 0 1 1.8E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 8.8E-03 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 1 6.4E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex 		201 0 1 5.0E-03 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C0241703
Disease: High pitched voice
High pitched voice 		35 0 1 2.8E-02 0 0
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		4173 0 1 2.4E-04 0 0
CUI: C0270911
Disease: Charcot-Marie-Tooth Disease, Type Ia (disorder)
Charcot-Marie-Tooth Disease, Type Ia (disorder) 		42 0 1 2.3E-02 0 0
CUI: C0270912
Disease: Charcot-Marie-Tooth Disease, Type Ib
Charcot-Marie-Tooth Disease, Type Ib 		12 0 1 7.7E-02 0 0
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 0 1 2.0E-02 0 0
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
Liver and Intrahepatic Biliary Tract Carcinoma 		1395 0 1 7.2E-04 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 4.4E-03 0 0