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: C0233623
Disease: Onychotillomania
Onychotillomania
1 0 1 0.50 0 0
CUI: C0752288
Disease: Adjustment Sleep Disorder
Adjustment Sleep Disorder
1 0 1 0.50 0 0
CUI: C0752289
Disease: Environmental Sleep Disorder
Environmental Sleep Disorder
1 0 1 0.50 0 0
CUI: C0752291
Disease: Limit-Setting Sleep Disorder
Limit-Setting Sleep Disorder
1 0 1 0.50 0 0
CUI: C0752292
Disease: Nocturnal Eating-Drinking Syndrome
Nocturnal Eating-Drinking Syndrome
1 0 1 0.50 0 0
CUI: C0752293
Disease: Sleep Disorders, Extrinsic
Sleep Disorders, Extrinsic
1 0 1 0.50 0 0
CUI: C2129647
Disease: menstrual symptoms
menstrual symptoms
1 0 1 0.50 0 0
CUI: C3661485
Disease: 17p11.2 Monosomy
17p11.2 Monosomy
1 0 1 0.50 0 0
CUI: C4014557
Disease: MYOPATHY, TUBULAR AGGREGATE, 2
MYOPATHY, TUBULAR AGGREGATE, 2
1 0 1 0.50 0 0
CUI: C4023493
Disease: Beta-EEG
Beta-EEG
1 0 1 0.50 0 0
CUI: C4023494
Disease: Alpha-EEG
Alpha-EEG
1 0 1 0.50 0 0
CUI: C4225255
Disease: YUAN-HAREL-LUPSKI SYNDROME
YUAN-HAREL-LUPSKI SYNDROME
1 0 1 0.50 0 0
CUI: C4703574
Disease: Sleep-wake inversion
Sleep-wake inversion
1 0 1 0.50 0 0
Infection by Pneumocystis jirovecii (disorder)
2 0 1 0.33 0 0
CUI: C1446787
Disease: Cramping sensation quality
Cramping sensation quality
2 0 1 0.33 0 0
EEG with focal epileptiform discharges
2 0 1 0.33 0 0
CUI: C1303009
Disease: Microcoria, congenital
Microcoria, congenital
3 0 1 0.25 0 0
CUI: C1861451
Disease: Stormorken Syndrome
Stormorken Syndrome
3 0 1 0.25 0 0
Immune dysfunction with T-cell inactivation due to calcium entry defect 2
3 0 1 0.25 0 0
CUI: C4011726
Disease: MYOPATHY, TUBULAR AGGREGATE, 1
MYOPATHY, TUBULAR AGGREGATE, 1
3 0 1 0.25 0 0
CUI: C0751901
Disease: Tic, Vocal
Tic, Vocal
4 0 1 0.20 0 0
CUI: C4021095
Disease: Abnormal hypothalamus morphology
Abnormal hypothalamus morphology
4 0 1 0.20 0 0
CUI: C4021391
Disease: Broad phalanges of the hand
Broad phalanges of the hand
4 0 1 0.20 0 0
Abnormal tracheobronchial morphology
4 0 1 0.20 0 0
CUI: C1844007
Disease: Corticospinal tract hypoplasia
Corticospinal tract hypoplasia
5 0 1 0.17 0 0