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: C4023690
Disease: Spontaneous pain sensation
Spontaneous pain sensation 		1 0 1 0.14 0 0
CUI: C4024933
Disease: Acute demyelinating polyneuropathy
Acute demyelinating polyneuropathy 		1 0 1 0.14 0 0
CUI: C4025027
Disease: Repeated pneumothoraces
Repeated pneumothoraces 		1 0 1 0.14 0 0
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME 		1 0 1 0.14 0 0
CUI: C4703574
Disease: Sleep-wake inversion
Sleep-wake inversion 		1 0 1 0.14 0 0
CUI: C0016579
Disease: Formication
Formication 		2 0 1 0.12 0 0
CUI: C0235044
Disease: Paresthesia, Distal
Paresthesia, Distal 		2 0 1 0.12 0 0
CUI: C0262576
Disease: Nerve paralysis
Nerve paralysis 		2 0 1 0.12 0 0
CUI: C0474520
Disease: Myokymia, Generalized
Myokymia, Generalized 		2 0 1 0.12 0 0
CUI: C0747708
Disease: Pneumothorax, recurrent
Pneumothorax, recurrent 		2 0 1 0.12 0 0
CUI: C0751412
Disease: Painful Paresthesias
Painful Paresthesias 		2 0 1 0.12 0 0
CUI: C0751460
Disease: Flaccid Quadriplegia
Flaccid Quadriplegia 		2 0 1 0.12 0 0
CUI: C0751461
Disease: Paralysis, Spinal, Quadriplegic
Paralysis, Spinal, Quadriplegic 		2 0 1 0.12 0 0
CUI: C0751922
Disease: Median Neuropathy
Median Neuropathy 		2 0 1 0.12 0 0
CUI: C1290871
Disease: Disorder of hand
Disorder of hand 		2 0 1 0.12 0 0
CUI: C1845165
Disease: PARKINSON DISEASE 12
PARKINSON DISEASE 12 		2 0 1 0.12 0 0
CUI: C1861675
Disease: Cold-induced muscle cramps
Cold-induced muscle cramps 		2 0 1 0.12 0 0
CUI: C2748568
Disease: Immune dysfunction with T-cell inactivation due to calcium entry defect 1
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 		2 0 1 0.12 0 0
CUI: C4016264
Disease: DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT
DEJERINE-SOTTAS SYNDROME, AUTOSOMAL DOMINANT 		2 0 1 0.12 0 0
CUI: C4021199
Disease: EEG with focal epileptiform discharges
EEG with focal epileptiform discharges 		2 0 1 0.12 0 0
CUI: C4275252
Disease: Familial spontaneous pneumothorax
Familial spontaneous pneumothorax 		2 0 1 0.12 0 0
CUI: C4518505
Disease: Partial trisomy of chromosome 17
Partial trisomy of chromosome 17 		2 0 1 0.12 0 0
CUI: C0206632
Disease: Angiolipoma
Angiolipoma 		3 0 1 0.11 0 0
CUI: C0555214
Disease: Multiple lung cysts
Multiple lung cysts 		3 0 1 0.11 0 0
CUI: C0596992
Disease: myelinopathy
myelinopathy 		3 0 1 0.11 0 0