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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance
0 1 0 0 1 1.8E-03
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency
0 1 0 0 1 1.8E-03
CUI: C0523550
Disease: Catalase measurement
Catalase measurement
0 2 0 0 1 1.8E-03
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A
0 1 0 0 1 1.8E-03
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait
0 2 0 0 1 1.8E-03
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 1.8E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 1.8E-03
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 1.8E-03
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement
0 8 0 0 1 1.8E-03
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 1.8E-03
CUI: C4050627
Disease: Soluble P-Selectin Measurement
Soluble P-Selectin Measurement
0 3 0 0 1 1.8E-03
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
249 742 1 1.9E-03 1 7.7E-04
CUI: C1854882
Disease: Absent speech
Absent speech
232 0 1 2.0E-03 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia
218 0 1 2.1E-03 0 0
CUI: C0020757
Disease: Ichthyoses
Ichthyoses
194 0 1 2.2E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 1 2.2E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 2.3E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 2.3E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear
152 0 1 2.4E-03 0 0
CUI: C0345392
Disease: Congenital kyphoscoliosis
Congenital kyphoscoliosis
151 0 1 2.4E-03 0 0
CUI: C0600033
Disease: Acquired Kyphoscoliosis
Acquired Kyphoscoliosis
149 0 1 2.4E-03 0 0
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
149 527 1 2.4E-03 1 9.3E-04
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 2.4E-03 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 1 2.4E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 526 1 2.4E-03 1 9.3E-04