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: C0276096
Disease: Mastitis-metritis-agalactia syndrome
Mastitis-metritis-agalactia syndrome 		23 0 6 0.18 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 4 0.15 0 0
CUI: C3151140
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 2D
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D 		7 0 3 0.14 0 0
CUI: C2717876
Disease: Propionicaciduria
Propionicaciduria 		2 0 2 0.12 0 0
CUI: C0241775
Disease: Organic aciduria
Organic aciduria 		12 0 3 0.12 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 3 0.11 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 3 0.11 0 0
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia 		5 0 2 1.0E-01 0 0
CUI: C3489576
Disease: Sexual Violence
Sexual Violence 		6 0 2 9.5E-02 0 0
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I 		18 0 3 9.4E-02 0 0
CUI: C4703632
Disease: Increased level of hippuric acid in urine
Increased level of hippuric acid in urine 		7 0 2 9.1E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 7 8.0E-02 0 0
CUI: C0041657
Disease: Unconscious State
Unconscious State 		13 0 2 7.1E-02 0 0
CUI: C0346991
Disease: Secondary malignant neoplasm of omentum
Secondary malignant neoplasm of omentum 		14 0 2 6.9E-02 0 0
CUI: C1306587
Disease: Acute encephalopathy
Acute encephalopathy 		31 0 3 6.7E-02 0 0
CUI: C4759295
Disease: Non-metastatic prostate cancer
Non-metastatic prostate cancer 		18 0 2 6.1E-02 0 0
CUI: C0022806
Disease: Kwashiorkor
Kwashiorkor 		19 0 2 5.9E-02 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 5.9E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 5.9E-02 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 5.9E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 5.9E-02 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 5.9E-02 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 5.9E-02 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 5.9E-02 0 0
CUI: C0268543
Disease: Hyperammonemia, type III
Hyperammonemia, type III 		1 0 1 5.9E-02 0 0