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: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0 51 0 0 1 1.5E-02
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0 51 0 0 1 1.5E-02
Atrophia Maculosa Varioliformis Cutis, Familial
0 1 0 0 1 6.7E-02
PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO
0 1 0 0 1 6.7E-02
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure
391 0 1 1.7E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.2E-03 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities
234 0 1 2.4E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 2.4E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 2.5E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead
211 0 1 2.5E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion
211 0 1 2.5E-03 0 0
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption
210 0 1 2.5E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.5E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 2.5E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry
206 0 1 2.5E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
595 0 2 2.6E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.6E-03 0 0
Abnormality of cardiovascular system morphology
198 0 1 2.6E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 2.6E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder
192 0 1 2.6E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum
182 25 1 2.7E-03 1 2.6E-02
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear
176 0 1 2.7E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia
172 0 1 2.8E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 2.8E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 2.8E-03 0 0