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: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		3 0 2 0.40 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 0.25 0 0
CUI: C0521663
Disease: Paraparesis, Chronic Progressive
Paraparesis, Chronic Progressive 		1 0 1 0.25 0 0
CUI: C0558193
Disease: Stiff limbs
Stiff limbs 		1 0 1 0.25 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 0.25 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 0.25 0 0
CUI: C1829648
Disease: Amino acidemias
Amino acidemias 		1 0 1 0.25 0 0
CUI: C2751494
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT 		1 0 1 0.25 0 0
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED 		1 0 1 0.25 0 0
CUI: C3536576
Disease: Chronic myelopathy
Chronic myelopathy 		1 0 1 0.25 0 0
CUI: C3888307
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT 		1 0 1 0.25 0 0
CUI: C3888308
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT 		1 0 1 0.25 0 0
CUI: C3888309
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT 		1 0 1 0.25 0 0
CUI: C4015785
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT 		1 0 1 0.25 0 0
CUI: C4017280
Disease: HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY
HYPERPHENYLALANINEMIA, BH4-DEFICIENT, A, DUE TO PARTIAL PTS DEFICIENCY 		1 0 1 0.25 0 0
CUI: C4025264
Disease: Recurrent cerebral hemorrhage
Recurrent cerebral hemorrhage 		1 0 1 0.25 0 0
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		1 0 1 0.25 0 0
CUI: C0035066
Disease: Renal Artery Obstruction
Renal Artery Obstruction 		2 0 1 0.20 0 0
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage 		2 0 1 0.20 0 0
CUI: C0600074
Disease: Autotomy
Autotomy 		2 0 1 0.20 0 0
CUI: C1282365
Disease: Mixed type cataract
Mixed type cataract 		2 0 1 0.20 0 0
CUI: C1411876
Disease: Developmental arithmetic disorder
Developmental arithmetic disorder 		2 0 1 0.20 0 0
CUI: C1562067
Disease: Human T-cell Lymphoma Virus Type -1 associated uveitis
Human T-cell Lymphoma Virus Type -1 associated uveitis 		2 0 1 0.20 0 0
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries 		2 0 1 0.20 0 0
CUI: C2930862
Disease: Primary angiitis of the central nervous system
Primary angiitis of the central nervous system 		2 0 1 0.20 0 0