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: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 1 1.7E-03 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate
611 0 1 1.6E-03 0 0
CUI: C0009024
Disease: Clonus
Clonus
60 0 1 1.7E-02 0 0
Congenital ocular coloboma (disorder)
129 0 1 7.8E-03 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
725 0 1 1.4E-03 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
33 0 1 3.0E-02 0 0
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
93 0 1 1.1E-02 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis
182 0 1 5.5E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
285 0 1 3.5E-03 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma
770 0 1 1.3E-03 0 0
Sensorineural Hearing Loss (disorder)
783 0 1 1.3E-03 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus
473 0 1 2.1E-03 0 0
CUI: C0022972
Disease: Lambert-Eaton Myasthenic Syndrome
Lambert-Eaton Myasthenic Syndrome
37 0 1 2.7E-02 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia
115 0 1 8.7E-03 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation
505 0 1 2.0E-03 0 0
CUI: C0025958
Disease: Microcephaly
Microcephaly
1064 0 1 9.4E-04 0 0
CUI: C0026010
Disease: Microphthalmos
Microphthalmos
337 0 1 3.0E-03 0 0
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation
340 0 1 2.9E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 5.1E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 0 1 1.0E-03 0 0
CUI: C0026848
Disease: Myopathy
Myopathy
634 0 1 1.6E-03 0 0
CUI: C0027092
Disease: Myopia
Myopia
490 0 1 2.0E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 1 1.2E-03 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy
568 0 1 1.8E-03 0 0