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: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 3.0E-02 0 0
CUI: C0009769
Disease: Conjunctivitis, Giant Papillary
Conjunctivitis, Giant Papillary
1 0 1 3.0E-02 0 0
CUI: C0009792
Disease: Consciousness Disorders
Consciousness Disorders
1 0 1 3.0E-02 0 0
CUI: C0019489
Disease: Deficiency, Hexosediphosphatase
Deficiency, Hexosediphosphatase
1 0 1 3.0E-02 0 0
CUI: C0019699
Disease: HIV Seropositivity
HIV Seropositivity
1 0 1 3.0E-02 0 0
CUI: C0030925
Disease: Peptic Ulcer Perforation
Peptic Ulcer Perforation
1 0 1 3.0E-02 0 0
Megaloblastic anemia due to folate deficiency
1 0 1 3.0E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria
1 0 1 3.0E-02 0 0
Secondary malignant neoplasm of adrenal gland
1 0 1 3.0E-02 0 0
CUI: C0155504
Disease: Serous labyrinthitis
Serous labyrinthitis
1 0 1 3.0E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement
1 0 1 3.0E-02 0 0
CUI: C0239778
Disease: Green urine
Green urine
1 0 1 3.0E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC
1 0 1 3.0E-02 0 0
CUI: C0266266
Disease: Congenital absence of pancreas
Congenital absence of pancreas
1 0 1 3.0E-02 0 0
CUI: C0267158
Disease: Reflux gastritis
Reflux gastritis
1 0 1 3.0E-02 0 0
Ketoacidosis due to acute alcohol intoxication
1 0 1 3.0E-02 0 0
Inherited disorder of bilirubin metabolism
1 0 1 3.0E-02 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia
1 0 1 3.0E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia
1 0 1 3.0E-02 0 0
CUI: C0276876
Disease: Infection by Leishmania infantum
Infection by Leishmania infantum
1 0 1 3.0E-02 0 0
CUI: C0277977
Disease: Murphy's sign
Murphy's sign
1 0 1 3.0E-02 0 0
CUI: C0333295
Disease: Acute ulcer
Acute ulcer
1 0 1 3.0E-02 0 0
recurrent childhood brain stem glioma
1 0 1 3.0E-02 0 0
CUI: C0339678
Disease: Simple myopia
Simple myopia
1 0 1 3.0E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness
1 0 1 3.0E-02 0 0