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: C0877104
Disease: Retinal toxicity
Retinal toxicity 		12 0 2 7.7E-02 0 0
CUI: C1836842
Disease: Psychomotor deterioration
Psychomotor deterioration 		13 0 2 7.4E-02 0 0
CUI: C0233762
Disease: Hallucinations, Auditory
Hallucinations, Auditory 		14 0 2 7.1E-02 0 0
CUI: C0422895
Disease: Primitive reflex
Primitive reflex 		14 0 2 7.1E-02 0 0
CUI: C1838319
Disease: Primitive reflexes (palmomental, snout, glabellar)
Primitive reflexes (palmomental, snout, glabellar) 		14 0 2 7.1E-02 0 0
CUI: C1866284
Disease: Motor deterioration
Motor deterioration 		14 0 2 7.1E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		77 0 6 6.9E-02 0 0
CUI: C0085078
Disease: Lysosomal Storage Diseases
Lysosomal Storage Diseases 		130 0 9 6.6E-02 0 0
CUI: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 6.2E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 6.2E-02 0 0
CUI: C0268274
Disease: Gangliosidoses, GM2
Gangliosidoses, GM2 		18 0 2 6.2E-02 0 0
CUI: C0854297
Disease: Head deformity
Head deformity 		1 0 1 6.2E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 0 1 6.2E-02 0 0
CUI: C1843014
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques 		1 0 1 6.2E-02 0 0
CUI: C1843015
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia 		1 0 1 6.2E-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 6.2E-02 0 0
CUI: C1864670
Disease: Neuronal Ceroid Lipofuscinosis, Congenital
Neuronal Ceroid Lipofuscinosis, Congenital 		1 0 1 6.2E-02 0 0
CUI: C3151038
Disease: ACNE INVERSA, FAMILIAL, 3
ACNE INVERSA, FAMILIAL, 3 		1 0 1 6.2E-02 0 0
CUI: C3160720
Disease: Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1u 		1 0 1 6.2E-02 0 0
CUI: C3715049
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 13
CEROID LIPOFUSCINOSIS, NEURONAL, 13 		1 0 1 6.2E-02 0 0
CUI: C4015371
Disease: MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT
MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT 		1 0 1 6.2E-02 0 0
CUI: C4015780
Disease: ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES
ALZHEIMER DISEASE, FAMILIAL, WITH SPASTIC PARAPARESIS AND UNUSUAL PLAQUES 		1 0 1 6.2E-02 0 0
CUI: C4015781
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES
ALZHEIMER DISEASE, FAMILIAL, 3, WITH UNUSUAL PLAQUES 		1 0 1 6.2E-02 0 0
CUI: C4015782
Disease: ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS
ALZHEIMER DISEASE, FAMILIAL, 3, WITH SPASTIC PARAPARESIS 		1 0 1 6.2E-02 0 0
CUI: C4017059
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED
CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED 		1 0 1 6.2E-02 0 0