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: C1840061
Disease: SMALL PATELLA SYNDROME
SMALL PATELLA SYNDROME 		21 0 4 0.15 0 0
CUI: C0031572
Disease: Phobia, Social
Phobia, Social 		33 0 5 0.13 0 0
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		9 0 2 0.12 0 0
CUI: C0236788
Disease: Bipolar II disorder
Bipolar II disorder 		21 0 3 0.11 0 0
CUI: C0023643
Disease: Lichen disease
Lichen disease 		33 0 4 0.10 0 0
CUI: C0003944
Disease: As If Personality
As If Personality 		1 0 1 1.0E-01 0 0
CUI: C0021124
Disease: Impulse-Ridden Personality
Impulse-Ridden Personality 		1 0 1 1.0E-01 0 0
CUI: C0021139
Disease: Inadequate Personality
Inadequate Personality 		1 0 1 1.0E-01 0 0
CUI: C0085292
Disease: Stiff-Person Syndrome
Stiff-Person Syndrome 		34 0 4 1.0E-01 0 0
CUI: C0086168
Disease: Dissociation
Dissociation 		1 0 1 1.0E-01 0 0
CUI: C0233461
Disease: Emotional impulsivity
Emotional impulsivity 		1 0 1 1.0E-01 0 0
CUI: C0233610
Disease: Negativism in catatonia
Negativism in catatonia 		1 0 1 1.0E-01 0 0
CUI: C0270587
Disease: Generalized social phobia
Generalized social phobia 		1 0 1 1.0E-01 0 0
CUI: C0349450
Disease: Soiling
Soiling 		1 1 1 1.0E-01 1 0.50
CUI: C0458631
Disease: Performance anxiety
Performance anxiety 		1 0 1 1.0E-01 0 0
CUI: C0679276
Disease: relief drinking
relief drinking 		1 0 1 1.0E-01 0 0
CUI: C1152136
Disease: sucrose-phosphate synthase activity
sucrose-phosphate synthase activity 		1 0 1 1.0E-01 0 0
CUI: C1840062
Disease: Hypoplasia of the lesser trochanter
Hypoplasia of the lesser trochanter 		1 0 1 1.0E-01 0 0
CUI: C1848680
Disease: 4-hydroxyphenylacetic aciduria
4-hydroxyphenylacetic aciduria 		1 0 1 1.0E-01 0 0
CUI: C1851734
Disease: Metopic ridge
Metopic ridge 		1 1 1 1.0E-01 1 0.50
CUI: C1868581
Disease: Patella aplasia, coxa vara, tarsal synostosis
Patella aplasia, coxa vara, tarsal synostosis 		1 0 1 1.0E-01 0 0
CUI: C2266670
Disease: ritualistic behavior (symptom)
ritualistic behavior (symptom) 		1 0 1 1.0E-01 0 0
CUI: C3150607
Disease: CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME
CHROMOSOME 17q23.1-q23.2 DELETION SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C3150880
Disease: CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME
CHROMOSOME 17q23.1-q23.2 DUPLICATION SYNDROME 		1 0 1 1.0E-01 0 0
CUI: C3553354
Disease: COENZYME Q10 DEFICIENCY, PRIMARY, 2
COENZYME Q10 DEFICIENCY, PRIMARY, 2 		1 0 1 1.0E-01 0 0