Source: ALL
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: C0009792
Disease: Consciousness Disorders
Consciousness Disorders 		1 0 1 1.8E-02 0 0
CUI: C0018814
Disease: Heart Rupture, Post-Infarction
Heart Rupture, Post-Infarction 		1 0 1 1.8E-02 0 0
CUI: C0019065
Disease: Hemoperitoneum
Hemoperitoneum 		1 0 1 1.8E-02 0 0
CUI: C0019250
Disease: Hereditary factor I deficiency disease
Hereditary factor I deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0019699
Disease: HIV Seropositivity
HIV Seropositivity 		1 0 1 1.8E-02 0 0
CUI: C0030925
Disease: Peptic Ulcer Perforation
Peptic Ulcer Perforation 		1 0 1 1.8E-02 0 0
CUI: C0085307
Disease: Embolism and Thrombosis
Embolism and Thrombosis 		1 0 1 1.8E-02 0 0
CUI: C0153691
Disease: Secondary malignant neoplasm of adrenal gland
Secondary malignant neoplasm of adrenal gland 		1 0 1 1.8E-02 0 0
CUI: C0153888
Disease: Chronic myeloid leukemia in remission
Chronic myeloid leukemia in remission 		1 0 1 1.8E-02 0 0
CUI: C0155504
Disease: Serous labyrinthitis
Serous labyrinthitis 		1 0 1 1.8E-02 0 0
CUI: C0162637
Disease: Strongylida Infections
Strongylida Infections 		1 0 1 1.8E-02 0 0
CUI: C0231618
Disease: Corkscrewing
Corkscrewing 		1 0 1 1.8E-02 0 0
CUI: C0234174
Disease: Sucking reflex
Sucking reflex 		1 0 1 1.8E-02 0 0
CUI: C0234966
Disease: Astasia
Astasia 		1 0 1 1.8E-02 0 0
CUI: C0238408
Disease: Hematoma of rectus sheath
Hematoma of rectus sheath 		1 0 1 1.8E-02 0 0
CUI: C0267158
Disease: Reflux gastritis
Reflux gastritis 		1 0 1 1.8E-02 0 0
CUI: C0267406
Disease: Mesenteric infarction
Mesenteric infarction 		1 0 1 1.8E-02 0 0
CUI: C0268039
Disease: Ketoacidosis due to acute alcohol intoxication
Ketoacidosis due to acute alcohol intoxication 		1 0 1 1.8E-02 0 0
CUI: C0269608
Disease: Antepartum hemorrhage
Antepartum hemorrhage 		1 0 1 1.8E-02 0 0
CUI: C0270027
Disease: Antepartum hemorrhage affecting fetus or newborn
Antepartum hemorrhage affecting fetus or newborn 		1 0 1 1.8E-02 0 0
CUI: C0272241
Disease: Complement abnormality
Complement abnormality 		1 0 1 1.8E-02 0 0
CUI: C0272272
Disease: Systemic fibrinogenolysis
Systemic fibrinogenolysis 		1 0 1 1.8E-02 0 0
CUI: C0272327
Disease: Hereditary factor X deficiency disease
Hereditary factor X deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0272328
Disease: Acquired factor X deficiency disease
Acquired factor X deficiency disease 		1 0 1 1.8E-02 0 0
CUI: C0272355
Disease: von Willebrand disease, type IIC
von Willebrand disease, type IIC 		1 0 1 1.8E-02 0 0