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: C0272263
Disease: Cryofibrinogenemia
Cryofibrinogenemia 		1 0 1 0.33 0 0
CUI: C0393968
Disease: Systemic lupus erythematosus encephalitis
Systemic lupus erythematosus encephalitis 		1 0 1 0.33 0 0
CUI: C0477365
Disease: Other specified degenerative diseases of nervous system
Other specified degenerative diseases of nervous system 		1 0 1 0.33 0 0
CUI: C3277693
Disease: Punctate vasculitis skin lesions
Punctate vasculitis skin lesions 		1 0 1 0.33 0 0
CUI: C4303564
Disease: Hereditary vascular retinopathy
Hereditary vascular retinopathy 		1 0 1 0.33 0 0
CUI: C4303791
Disease: Cerebroretinal vasculopathy
Cerebroretinal vasculopathy 		1 0 1 0.33 0 0
CUI: C0271899
Disease: Normocytic normochromic anemia
Normocytic normochromic anemia 		2 0 1 0.25 0 0
CUI: C0427877
Disease: Cerebrospinal fluid lymphocytosis
Cerebrospinal fluid lymphocytosis 		2 0 1 0.25 0 0
CUI: C1835916
Disease: AICARDI-GOUTIERES SYNDROME 3
AICARDI-GOUTIERES SYNDROME 3 		2 0 1 0.25 0 0
CUI: C1856979
Disease: Deep white matter hypodensities
Deep white matter hypodensities 		2 0 1 0.25 0 0
CUI: C1856983
Disease: Increased CSF interferon alpha
Increased CSF interferon alpha 		7 0 2 0.25 0 0
CUI: C1860518
Disease: Vasculopathy, Retinal, With Cerebral Leukodystrophy
Vasculopathy, Retinal, With Cerebral Leukodystrophy 		2 0 1 0.25 0 0
CUI: C2749659
Disease: AICARDI-GOUTIERES SYNDROME 5 (disorder)
AICARDI-GOUTIERES SYNDROME 5 (disorder) 		2 0 1 0.25 0 0
CUI: C3150315
Disease: AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT
AICARDI-GOUTIERES SYNDROME 1, AUTOSOMAL DOMINANT 		2 0 1 0.25 0 0
CUI: C3539013
Disease: AICARDI-GOUTIERES SYNDROME 6
AICARDI-GOUTIERES SYNDROME 6 		2 0 1 0.25 0 0
CUI: C3888244
Disease: AICARDI-GOUTIERES SYNDROME 7
AICARDI-GOUTIERES SYNDROME 7 		2 0 1 0.25 0 0
CUI: C4021148
Disease: Abnormality of the medulla oblongata
Abnormality of the medulla oblongata 		2 0 1 0.25 0 0
CUI: C4024229
Disease: Chronic CSF lymphocytosis
Chronic CSF lymphocytosis 		7 0 2 0.25 0 0
CUI: C4072900
Disease: Increased serum interferon-gamma level
Increased serum interferon-gamma level 		7 0 2 0.25 0 0
CUI: C4748927
Disease: MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS
MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS 		2 0 1 0.25 0 0
CUI: C3277688
Disease: Progressive forgetfulness
Progressive forgetfulness 		3 0 1 0.20 0 0
CUI: C4022417
Disease: Degeneration of the striatum
Degeneration of the striatum 		9 0 2 0.20 0 0
CUI: C1833434
Disease: Multifocal cerebral white matter abnormalities
Multifocal cerebral white matter abnormalities 		10 0 2 0.18 0 0
CUI: C4023169
Disease: Moyamoya phenomenon
Moyamoya phenomenon 		10 0 2 0.18 0 0
CUI: C1852470
Disease: Extrapyramidal muscular rigidity
Extrapyramidal muscular rigidity 		11 0 2 0.17 0 0