Source: CURATED ×
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: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation 		4 0 4 1.00 0 0
CUI: C0026205
Disease: Miosis disorder
Miosis disorder 		1 0 1 0.25 0 0
CUI: C0038441
Disease: Stress Disorders, Traumatic
Stress Disorders, Traumatic 		1 0 1 0.25 0 0
CUI: C0039070
Disease: Syncope
Syncope 		1 0 1 0.25 0 0
CUI: C0700201
Disease: Dyssomnias
Dyssomnias 		1 0 1 0.25 0 0
CUI: C0752288
Disease: Adjustment Sleep Disorder
Adjustment Sleep Disorder 		1 0 1 0.25 0 0
CUI: C0752289
Disease: Environmental Sleep Disorder
Environmental Sleep Disorder 		1 0 1 0.25 0 0
CUI: C0752291
Disease: Limit-Setting Sleep Disorder
Limit-Setting Sleep Disorder 		1 0 1 0.25 0 0
CUI: C0752292
Disease: Nocturnal Eating-Drinking Syndrome
Nocturnal Eating-Drinking Syndrome 		1 0 1 0.25 0 0
CUI: C0752293
Disease: Sleep Disorders, Extrinsic
Sleep Disorders, Extrinsic 		1 0 1 0.25 0 0
CUI: C1832916
Disease: Timothy syndrome
Timothy syndrome 		1 0 1 0.25 0 0
CUI: C1850077
Disease: Supranuclear Palsy, Progressive, 1, Atypical
Supranuclear Palsy, Progressive, 1, Atypical 		1 0 1 0.25 0 0
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 0.25 0 0
CUI: C3661485
Disease: 17p11.2 Monosomy
17p11.2 Monosomy 		1 0 1 0.25 0 0
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME 		1 0 1 0.25 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		2 0 1 0.20 0 0
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		2 0 1 0.20 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 0.20 0 0
CUI: C2931246
Disease: Potocki-Lupski syndrome
Potocki-Lupski syndrome 		2 0 1 0.20 0 0
CUI: C0949664
Disease: Tauopathies
Tauopathies 		3 0 1 0.17 0 0
CUI: C0268849
Disease: Overactive Detrusor
Overactive Detrusor 		4 0 1 0.14 0 0
CUI: C0795864
Disease: Smith-Magenis syndrome
Smith-Magenis syndrome 		4 0 1 0.14 0 0
CUI: C0878773
Disease: Overactive Bladder
Overactive Bladder 		4 0 1 0.14 0 0
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		6 0 1 0.11 0 0
CUI: C4551862
Disease: Ophthalmoplegia, Progressive Supranuclear
Ophthalmoplegia, Progressive Supranuclear 		6 0 1 0.11 0 0