Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 4.8E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 9.5E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 4.8E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 2 1.7E-03 0 0
Creatine phosphokinase serum increased
228 0 1 1.9E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 1.9E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears
223 0 1 1.9E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 2.0E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance
211 0 1 2.0E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 2.0E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.0E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria
199 0 1 2.0E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 2.1E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge
180 0 1 2.1E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 1 2.2E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.2E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
156 0 1 2.2E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 1 2.3E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity
147 0 1 2.3E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 2.3E-03 0 0
CUI: C0158731
Disease: Congenital pectus carinatum
Congenital pectus carinatum
138 0 1 2.3E-03 0 0
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
565 0 2 2.3E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 2.3E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 2.4E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay
130 0 1 2.4E-03 0 0