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: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 5.3E-02 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 5.3E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 5.3E-02 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 5.3E-02 0 0
CUI: C0266445
Disease: Congenital atresia of vas deferens
Congenital atresia of vas deferens 		1 0 1 5.3E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 5.3E-02 0 0
CUI: C0269852
Disease: Vasa Previa
Vasa Previa 		1 0 1 5.3E-02 0 0
CUI: C0271294
Disease: Chronic allergic conjunctivitis
Chronic allergic conjunctivitis 		1 0 1 5.3E-02 0 0
CUI: C0334390
Disease: Acinar cell tumor
Acinar cell tumor 		1 0 1 5.3E-02 0 0
CUI: C0343972
Disease: Schistosomal splenomegaly
Schistosomal splenomegaly 		1 0 1 5.3E-02 0 0
CUI: C0392180
Disease: Necrosis of placenta
Necrosis of placenta 		1 0 1 5.3E-02 0 0
CUI: C0400973
Disease: Synthetic defect of bile acids
Synthetic defect of bile acids 		1 0 1 5.3E-02 0 0
CUI: C0431603
Disease: Ectopic liver
Ectopic liver 		1 0 1 5.3E-02 0 0
CUI: C0743188
Disease: diarrhea persistent
diarrhea persistent 		1 0 1 5.3E-02 0 0
CUI: C1167752
Disease: Graft ischaemia
Graft ischaemia 		1 0 1 5.3E-02 0 0
CUI: C1332316
Disease: Apocrine breast carcinoma
Apocrine breast carcinoma 		1 0 1 5.3E-02 0 0
CUI: C1335461
Disease: Postsurgical Stage I Hepatoblastoma
Postsurgical Stage I Hepatoblastoma 		1 0 1 5.3E-02 0 0
CUI: C1567427
Disease: Bilateral Multicystic Dysplastic Kidneys
Bilateral Multicystic Dysplastic Kidneys 		1 0 1 5.3E-02 0 0
CUI: C1843116
Disease: Bile acid synthesis defect, congenital, 1
Bile acid synthesis defect, congenital, 1 		1 0 1 5.3E-02 0 0
CUI: C1863080
Disease: ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF
ALPHA-FETOPROTEIN, HEREDITARY PERSISTENCE OF 		1 0 1 5.3E-02 0 0
CUI: C1863081
Disease: alpha-Fetoprotein Deficiency
alpha-Fetoprotein Deficiency 		1 0 1 5.3E-02 0 0
CUI: C3665817
Disease: Hypocarnitinaemia
Hypocarnitinaemia 		1 0 1 5.3E-02 0 0
CUI: C3890733
Disease: Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Positive
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Positive 		1 0 1 5.3E-02 0 0
CUI: C4022148
Disease: Abnormality of the dentate nucleus
Abnormality of the dentate nucleus 		1 0 1 5.3E-02 0 0
CUI: C4022163
Disease: Abnormality of central somatosensory evoked potentials
Abnormality of central somatosensory evoked potentials 		1 0 1 5.3E-02 0 0