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: C0023066
Disease: Laryngospasm
Laryngospasm 		48 0 1 1.2E-03 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 1.2E-03 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 1.2E-03 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 1.2E-03 0 0
CUI: C2931498
Disease: Mental Retardation, X-Linked 1
Mental Retardation, X-Linked 1 		45 0 1 1.2E-03 0 0
CUI: C0427055
Disease: Facial Paresis
Facial Paresis 		44 0 1 1.2E-03 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 1.2E-03 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy 		42 0 1 1.2E-03 0 0
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		42 0 1 1.2E-03 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 1 1.2E-03 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis 		42 0 1 1.2E-03 0 0
CUI: C0426818
Disease: Thin rib
Thin rib 		42 0 1 1.2E-03 0 0
CUI: C0751093
Disease: Dystonia, Limb
Dystonia, Limb 		42 0 1 1.2E-03 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 1 1.2E-03 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 1.2E-03 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia 		41 0 1 1.2E-03 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 1 1.2E-03 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 1.2E-03 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 1 1.2E-03 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 1.2E-03 0 0
CUI: C1837522
Disease: Impaired pain sensation
Impaired pain sensation 		41 0 1 1.2E-03 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 1 1.2E-03 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia 		41 0 1 1.2E-03 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 1.2E-03 0 0
CUI: C4021741
Disease: Abnormal cortical bone morphology
Abnormal cortical bone morphology 		41 0 1 1.2E-03 0 0