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: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		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: C1859817
Disease: 2-AMINOADIPIC 2-OXOADIPIC ACIDURIA
2-AMINOADIPIC 2-OXOADIPIC ACIDURIA 		1 0 1 0.25 0 0
CUI: C2733049
Disease: Alpha ketoadipic aciduria
Alpha ketoadipic aciduria 		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: 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: C4012597
Disease: ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE
ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE 		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: C4021548
Disease: Adrenocorticotropin receptor defect
Adrenocorticotropin receptor defect 		1 0 1 0.25 0 0
CUI: C4025264
Disease: Recurrent cerebral hemorrhage
Recurrent cerebral hemorrhage 		1 0 1 0.25 0 0
CUI: C4538604
Disease: Alpha-aminoadipic aciduria
Alpha-aminoadipic aciduria 		1 0 1 0.25 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: C1411876
Disease: Developmental arithmetic disorder
Developmental arithmetic disorder 		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
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency 		3 0 1 0.17 0 0
CUI: C1527338
Disease: Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type 		3 0 1 0.17 0 0
CUI: C2363813
Disease: Short-term memory impairment
Short-term memory impairment 		3 0 1 0.17 0 0
CUI: C2931257
Disease: Alzheimer disease type 1
Alzheimer disease type 1 		3 0 1 0.17 0 0
CUI: C4023807
Disease: Abnormality of the hypothenar eminence
Abnormality of the hypothenar eminence 		3 0 1 0.17 0 0