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: C0268958
Disease: Acute orchitis
Acute orchitis
0 1 0 0 1 1.3E-02
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania
0 1 0 0 1 1.3E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 1.3E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 1.3E-02
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain
0 2 0 0 1 1.3E-02
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia
0 4 0 0 1 1.3E-02
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1
0 6 0 0 2 2.5E-02
Frequent episodic tension-type headache
0 1 0 0 1 1.3E-02
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
149 0 1 2.1E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
147 0 1 2.1E-03 0 0
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
147 0 1 2.1E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
147 0 1 2.1E-03 0 0
CUI: C0005845
Disease: Blood urea nitrogen measurement
Blood urea nitrogen measurement
90 0 1 2.3E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
87 0 1 2.4E-03 0 0
Autosomal recessive retinitis pigmentosa
82 0 1 2.4E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement
82 0 1 2.4E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion
79 0 1 2.4E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk
77 0 1 2.4E-03 0 0
CUI: C0262630
Disease: Reduced concentration span
Reduced concentration span
77 2 1 2.4E-03 1 1.3E-02
CUI: C3554617
Disease: Adducted thumb
Adducted thumb
74 0 1 2.4E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact
73 0 1 2.4E-03 0 0
CUI: C0162351
Disease: Contact hypersensitivity
Contact hypersensitivity
71 0 1 2.5E-03 0 0
CUI: C0426415
Disease: Large nose
Large nose
70 7 1 2.5E-03 1 1.2E-02
CUI: C0426848
Disease: Sacral dimple
Sacral dimple
69 0 1 2.5E-03 0 0
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
66 0 1 2.5E-03 0 0