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: C0004134
Disease: Ataxia
Ataxia 		868 0 1 1.2E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 0 1 2.3E-03 0 0
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		852 0 2 2.3E-03 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 0 1 2.6E-03 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 1 2.0E-03 0 0
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		143 0 1 6.9E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		770 0 1 1.3E-03 0 0
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 1 1.3E-03 0 0
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		978 0 2 2.0E-03 0 0
CUI: C0021359
Disease: Infertility
Infertility 		130 0 1 7.6E-03 0 0
CUI: C0021364
Disease: Male infertility
Male infertility 		516 0 1 1.9E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 1.5E-02 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		340 0 1 2.9E-03 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 0 1 1.7E-03 0 0
CUI: C0027651
Disease: Neoplasms
Neoplasms 		10161 0 1 9.8E-05 0 0
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		977 0 1 1.0E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus 		833 0 1 1.2E-03 0 0
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		2078 0 1 4.8E-04 0 0
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 0 1 5.0E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 4.6E-03 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		850 0 1 1.2E-03 0 0
CUI: C0037771
Disease: Paraparesis, Spastic
Paraparesis, Spastic 		75 0 1 1.3E-02 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 6.9E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 8.1E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 4.7E-03 0 0