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: C0021704
Disease: Intelligence
Intelligence
645 0 1 1.3E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 2.4E-03 0 0
Creatine phosphokinase serum increased
228 0 1 2.7E-03 0 0
Platelet mean volume determination (procedure)
223 0 1 2.7E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 1 2.8E-03 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic
209 0 1 2.8E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry
206 0 1 2.9E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.9E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 3.0E-03 0 0
Malformations of Cortical Development, Group II
180 0 1 3.1E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 3.2E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive
172 0 1 3.2E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 3.2E-03 0 0
Child Development Disorders, Pervasive
168 0 1 3.2E-03 0 0
CUI: C0008489
Disease: Chorea
Chorea
168 0 1 3.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 3.2E-03 0 0
CUI: C0393593
Disease: Dystonia Disorders
Dystonia Disorders
167 0 1 3.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 3.3E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 3.3E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
156 0 1 3.4E-03 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome
150 0 1 3.4E-03 0 0
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
149 0 1 3.4E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 3.4E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia
148 0 1 3.4E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 0 1 3.5E-03 0 0