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: C0018810
Disease: heart rate
heart rate
0 103 0 0 1 8.6E-03
CUI: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.4E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability
854 0 2 2.1E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression
333 0 1 2.4E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency
315 0 1 2.5E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy
305 0 1 2.6E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck
288 0 1 2.7E-03 0 0
CUI: C1305855
Disease: Body mass index
Body mass index
1014 0 3 2.8E-03 0 0
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
272 0 1 2.9E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.9E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 2.9E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.9E-03 0 0
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
578 0 2 3.1E-03 0 0
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 0 1 3.1E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 3.2E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
868 0 3 3.2E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 3.2E-03 0 0
Creatine phosphokinase serum increased
228 0 1 3.3E-03 0 0
CUI: C0151611
Disease: Electroencephalogram abnormal
Electroencephalogram abnormal
227 0 1 3.3E-03 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus
833 0 3 3.3E-03 0 0
CUI: C0311394
Disease: Difficulty walking
Difficulty walking
224 0 1 3.3E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 3.3E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 1 3.4E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure
216 0 1 3.4E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 3.4E-03 0 0