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: C0009398
Disease: Color vision defect
Color vision defect
0 4 0 0 2 2.9E-02
CUI: C0234253
Disease: Rest pain
Rest pain
0 1 0 0 1 1.5E-02
CUI: C0236048
Disease: Polyposis, Gastric
Polyposis, Gastric
0 4 0 0 1 1.4E-02
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F
0 31 0 0 1 1.0E-02
CUI: C0343640
Disease: African Burkitt's lymphoma
African Burkitt's lymphoma
0 5 0 0 1 1.4E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 1.5E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 1.5E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 1.5E-02
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder)
0 1 0 0 1 1.5E-02
CUI: C2076602
Disease: Influenza A (H3N2)
Influenza A (H3N2)
0 1 0 0 1 1.5E-02
CUI: C2945759
Disease: aggressive cancer
aggressive cancer
0 5 0 0 2 2.9E-02
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism
0 2 0 0 1 1.5E-02
Frequent episodic tension-type headache
0 1 0 0 1 1.5E-02
Corpuscular Hemoglobin Concentration Mean
401 0 1 2.0E-03 0 0
CUI: C0520947
Disease: Clumsiness - motor delay
Clumsiness - motor delay
393 0 1 2.1E-03 0 0
CUI: C1854301
Disease: Motor delay
Motor delay
384 0 1 2.1E-03 0 0
CUI: C0221354
Disease: Frontal bossing
Frontal bossing
321 0 1 2.4E-03 0 0
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy
321 0 1 2.4E-03 0 0
CUI: C3806482
Disease: Recurrent respiratory infections
Recurrent respiratory infections
318 0 1 2.4E-03 0 0
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
681 0 2 2.6E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot
285 0 1 2.6E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 0 1 2.7E-03 0 0
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
610 0 2 2.8E-03 0 0
CUI: C0489786
Disease: Height
Height
249 0 1 2.9E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 3.0E-03 0 0