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: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy
0 120 0 0 1 6.8E-03
CUI: C0342546
Disease: Premature adrenarche
Premature adrenarche
0 11 0 0 2 5.6E-02
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess
0 3 0 0 1 3.4E-02
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF
0 1 0 0 1 3.7E-02
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF
0 1 0 0 1 3.7E-02
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
0 1 0 0 1 3.7E-02
CUI: C2712907
Disease: obsolete Combined hyperlipidemia
obsolete Combined hyperlipidemia
0 4 0 0 2 6.9E-02
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
0 1 0 0 1 3.7E-02
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties
473 0 1 1.7E-03 0 0
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 0 1 1.8E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking
391 0 1 1.9E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.0E-03 0 0
CUI: C1861403
Disease: Variable expressivity
Variable expressivity
319 0 1 2.3E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
291 0 1 2.4E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
285 0 1 2.4E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.6E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence
645 2093 2 2.6E-03 1 4.7E-04
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
251 0 1 2.7E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 2.7E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 2.7E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.8E-03 0 0
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
234 0 1 2.8E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 2.8E-03 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
228 0 1 2.8E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia
226 0 1 2.9E-03 0 0