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: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 0 7 0.12 0 0
CUI: C4022588
Disease: Fatigable weakness of swallowing muscles
Fatigable weakness of swallowing muscles 		39 0 6 0.12 0 0
CUI: C0393554
Disease: Amyotrophic Lateral Sclerosis With Dementia
Amyotrophic Lateral Sclerosis With Dementia 		30 0 5 0.11 0 0
CUI: C0205858
Disease: General Paralysis
General Paralysis 		12 0 3 0.11 0 0
CUI: C4082769
Disease: Chronic Traumatic Encephalopathy
Chronic Traumatic Encephalopathy 		12 0 3 0.11 0 0
CUI: C0023355
Disease: Leptomeningitis
Leptomeningitis 		2 0 2 0.11 0 0
CUI: C0038538
Disease: Subdural Effusion
Subdural Effusion 		2 0 2 0.11 0 0
CUI: C0153167
Disease: Neurosyphilis, Asymptomatic
Neurosyphilis, Asymptomatic 		2 0 2 0.11 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 4 0.11 0 0
CUI: C0269199
Disease: Stenosis of cervix
Stenosis of cervix 		2 0 2 0.11 0 0
CUI: C0270687
Disease: Pseudomeningocele
Pseudomeningocele 		2 0 2 0.11 0 0
CUI: C0270697
Disease: Post-Lumbar Puncture Headache
Post-Lumbar Puncture Headache 		2 0 2 0.11 0 0
CUI: C0270764
Disease: Motor Neuron Disease, Lower
Motor Neuron Disease, Lower 		23 0 4 0.11 0 0
CUI: C0338424
Disease: Bacterial encephalitis
Bacterial encephalitis 		2 0 2 0.11 0 0
CUI: C0431357
Disease: External hydrocephalus
External hydrocephalus 		2 0 2 0.11 0 0
CUI: C0494053
Disease: Neurosyphilis, Symptomatic
Neurosyphilis, Symptomatic 		2 0 2 0.11 0 0
CUI: C0751188
Disease: Post-Dural Puncture Headaches
Post-Dural Puncture Headaches 		2 0 2 0.11 0 0
CUI: C0751732
Disease: Intracranial Hypotension, Secondary
Intracranial Hypotension, Secondary 		2 0 2 0.11 0 0
CUI: C0848598
Disease: Nerve root irritation
Nerve root irritation 		2 0 2 0.11 0 0
CUI: C0848633
Disease: Sinus pressure
Sinus pressure 		2 0 2 0.11 0 0
CUI: C1336829
Disease: Tuberculum Sellae Meningioma
Tuberculum Sellae Meningioma 		2 0 2 0.11 0 0
CUI: C1735911
Disease: Weakness worsened
Weakness worsened 		2 0 2 0.11 0 0
CUI: C1838069
Disease: SCHIZOPHRENIA 3 (disorder)
SCHIZOPHRENIA 3 (disorder) 		2 0 2 0.11 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 2 0.11 0 0
CUI: C3151343
Disease: SPINOCEREBELLAR ATAXIA 32
SPINOCEREBELLAR ATAXIA 32 		2 0 2 0.11 0 0