Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Refractory anaemia with excess blasts
0 2 0 0 1 4.0E-02
CUI: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome
0 3 0 0 1 3.8E-02
CUI: C0033246
Disease: Proctitis
Proctitis
0 2 0 0 1 4.0E-02
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood
0 20 0 0 1 2.3E-02
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia
0 2 0 0 1 4.0E-02
CUI: C0242453
Disease: Prostatism
Prostatism
0 1 0 0 1 4.2E-02
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 4.2E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 3.3E-02
CUI: C0278139
Disease: Moderate pain
Moderate pain
0 1 0 0 1 4.2E-02
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma
0 6 0 0 1 3.4E-02
CUI: C0393761
Disease: Middle insomnia
Middle insomnia
0 1 0 0 1 4.2E-02
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 4.0E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
0 2 0 0 1 4.0E-02
CUI: C0948698
Disease: Coronary spastic angina
Coronary spastic angina
0 1 0 0 1 4.2E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 4.0E-02
Refractory anemia with ringed sideroblasts
0 3 0 0 1 3.8E-02
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
0 1 0 0 1 4.2E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 3.1E-02
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse
0 1 0 0 1 4.2E-02
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
0 1 0 0 1 4.2E-02
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7
0 6 0 0 1 3.4E-02
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia
0 4 0 0 1 3.7E-02
Frequent episodic tension-type headache
0 1 0 0 1 4.2E-02
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
Stage IV Prostate Cancer AJCC v8
0 6 0 0 1 3.4E-02
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia
312 0 1 2.1E-03 0 0