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: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 1.9E-02 0 0
CUI: C0014127
Disease: Endocervicitis
Endocervicitis 		1 0 1 1.9E-02 0 0
CUI: C0014574
Disease: Epiphysitis
Epiphysitis 		1 0 1 1.9E-02 0 0
CUI: C0029291
Disease: Psittacosis
Psittacosis 		1 0 1 1.9E-02 0 0
CUI: C0040559
Disease: Toxoplasmosis, Animal
Toxoplasmosis, Animal 		1 0 1 1.9E-02 0 0
CUI: C0085388
Disease: Intracranial Tuberculoma
Intracranial Tuberculoma 		1 0 1 1.9E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 1.9E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.9E-02 0 0
CUI: C0151536
Disease: Stenosis of bronchus
Stenosis of bronchus 		1 0 1 1.9E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 1.9E-02 0 0
CUI: C0155380
Disease: Dissociated Nystagmus
Dissociated Nystagmus 		1 0 1 1.9E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.9E-02 0 0
CUI: C0221360
Disease: Congenital absence of diaphragm
Congenital absence of diaphragm 		1 0 1 1.9E-02 0 0
CUI: C0233599
Disease: Bar-biting
Bar-biting 		1 0 1 1.9E-02 0 0
CUI: C0235453
Disease: Steroid withdrawal syndrome
Steroid withdrawal syndrome 		1 0 1 1.9E-02 0 0
CUI: C0235876
Disease: Depression aggravated
Depression aggravated 		1 0 1 1.9E-02 0 0
CUI: C0238120
Disease: Acquired Factor XIII Deficiency
Acquired Factor XIII Deficiency 		1 0 1 1.9E-02 0 0
CUI: C0238309
Disease: Ischemic peripheral neuropathy
Ischemic peripheral neuropathy 		1 0 1 1.9E-02 0 0
CUI: C0238741
Disease: Upper back pain
Upper back pain 		1 0 1 1.9E-02 0 0
CUI: C0238814
Disease: brain hemangioma
brain hemangioma 		1 0 1 1.9E-02 0 0
CUI: C0240709
Disease: Pericardial constriction
Pericardial constriction 		1 0 1 1.9E-02 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 1.9E-02 0 0
CUI: C0265831
Disease: Congenital absence of pulmonic valve
Congenital absence of pulmonic valve 		1 0 1 1.9E-02 0 0
CUI: C0266782
Disease: Abnormal yolk sac
Abnormal yolk sac 		1 0 1 1.9E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 1.9E-02 0 0