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: C0018975
Disease: Hemeralopia
Hemeralopia 		12 0 2 6.9E-02 0 0
CUI: C0877104
Disease: Retinal toxicity
Retinal toxicity 		12 0 2 6.9E-02 0 0
CUI: C1836842
Disease: Psychomotor deterioration
Psychomotor deterioration 		13 0 2 6.7E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		77 0 6 6.7E-02 0 0
CUI: C1866284
Disease: Motor deterioration
Motor deterioration 		14 0 2 6.5E-02 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases 		130 0 9 6.4E-02 0 0
CUI: C1846142
Disease: HOYERAAL-HREIDARSSON SYNDROME
HOYERAAL-HREIDARSSON SYNDROME 		16 0 2 6.1E-02 0 0
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita 		17 0 2 5.9E-02 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 2 5.7E-02 0 0
CUI: C0271185
Disease: Metamorphopsia
Metamorphopsia 		18 0 2 5.7E-02 0 0
CUI: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 5.3E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 5.3E-02 0 0
CUI: C0854297
Disease: Head deformity
Head deformity 		1 0 1 5.3E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 6 1 5.3E-02 1 0.11
CUI: C1843164
Disease: Charcot-Marie-Tooth disease, demyelinating, Type 1F
Charcot-Marie-Tooth disease, demyelinating, Type 1F 		1 0 1 5.3E-02 0 0
CUI: C1843169
Disease: Clusters of axonal regeneration
Clusters of axonal regeneration 		1 0 1 5.3E-02 0 0
CUI: C1843225
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder) 		1 0 1 5.3E-02 0 0
CUI: C1843885
Disease: Progressive gait ataxia
Progressive gait ataxia 		21 0 2 5.3E-02 0 0
CUI: C1864669
Disease: NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY
NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C1864670
Disease: Neuronal Ceroid Lipofuscinosis, Congenital
Neuronal Ceroid Lipofuscinosis, Congenital 		1 0 1 5.3E-02 0 0
CUI: C4015371
Disease: MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT
MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT 		1 0 1 5.3E-02 0 0
CUI: C4016662
Disease: ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C4016663
Disease: ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C4017059
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED
CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED 		1 0 1 5.3E-02 0 0
CUI: C4225283
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7 		1 0 1 5.3E-02 0 0