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: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		5 0 2 0.15 0 0
CUI: C0524812
Disease: Intracranial Hypotension
Intracranial Hypotension 		5 0 2 0.15 0 0
CUI: C0917814
Disease: Aphasia, Expressive
Aphasia, Expressive 		5 0 2 0.15 0 0
CUI: C1141920
Disease: Shunt infection
Shunt infection 		5 0 2 0.15 0 0
CUI: C1265713
Disease: Trephine hole
Trephine hole 		5 0 2 0.15 0 0
CUI: C3544214
Disease: Reversible cerebral vasoconstriction syndrome
Reversible cerebral vasoconstriction syndrome 		5 0 2 0.15 0 0
CUI: C3825276
Disease: Stereotyped behavior (Psychiatry)
Stereotyped behavior (Psychiatry) 		5 0 2 0.15 0 0
CUI: C4477058
Disease: Fragmented sleep
Fragmented sleep 		5 0 2 0.15 0 0
CUI: C0032268
Disease: Pneumocephalus
Pneumocephalus 		6 0 2 0.14 0 0
CUI: C0266476
Disease: Congenital stenosis of aqueduct of Sylvius
Congenital stenosis of aqueduct of Sylvius 		6 0 2 0.14 0 0
CUI: C0338582
Disease: Sporadic Cerebral Amyloid Angiopathy
Sporadic Cerebral Amyloid Angiopathy 		6 0 2 0.14 0 0
CUI: C0746495
Disease: Recurrent meningitis
Recurrent meningitis 		6 0 2 0.14 0 0
CUI: C1334240
Disease: Intracranial Germinoma
Intracranial Germinoma 		6 0 2 0.14 0 0
CUI: C1456865
Disease: Ureteral Calculi
Ureteral Calculi 		6 0 2 0.14 0 0
CUI: C4316985
Disease: Cerebellar edema
Cerebellar edema 		6 0 2 0.14 0 0
CUI: C0010266
Disease: Cranial nerve diseases
Cranial nerve diseases 		7 0 2 0.13 0 0
CUI: C0266456
Disease: Meningoencephalocele
Meningoencephalocele 		7 0 2 0.13 0 0
CUI: C0276430
Disease: Enterovirus meningitis
Enterovirus meningitis 		7 0 2 0.13 0 0
CUI: C0348165
Disease: Central Nervous System Viral Diseases
Central Nervous System Viral Diseases 		7 0 2 0.13 0 0
CUI: C0393547
Disease: Bulbospinal Neuronopathy
Bulbospinal Neuronopathy 		7 0 2 0.13 0 0
CUI: C0751186
Disease: Orthostatic Headache
Orthostatic Headache 		7 0 2 0.13 0 0
CUI: C1850380
Disease: NEUTROPHIL ACTIN DYSFUNCTION
NEUTROPHIL ACTIN DYSFUNCTION 		7 0 2 0.13 0 0
CUI: C1868117
Disease: POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA
POLYDACTYLY, POSTAXIAL, WITH PROGRESSIVE MYOPIA 		7 0 2 0.13 0 0
CUI: C2220255
Disease: Motor disturbances
Motor disturbances 		16 0 3 0.13 0 0
CUI: C0026976
Disease: Myelitis, Transverse
Myelitis, Transverse 		8 0 2 0.12 0 0