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: C0268623
Disease: Tyrosinemia, Type III
Tyrosinemia, Type III 		4 0 4 0.22 0 0
CUI: C0268487
Disease: Tyrosine Transaminase Deficiency Disease
Tyrosine Transaminase Deficiency Disease 		7 0 3 0.14 0 0
CUI: C0268483
Disease: Tyrosinemias
Tyrosinemias 		17 3 4 0.13 3 5.4E-02
CUI: C0406161
Disease: Seed corn
Seed corn 		2 0 2 0.11 0 0
CUI: C1291607
Disease: Deficiency of maleylacetoacetate isomerase
Deficiency of maleylacetoacetate isomerase 		2 0 2 0.11 0 0
CUI: C1848678
Disease: 4-Hydroxyphenylpyruvic aciduria
4-Hydroxyphenylpyruvic aciduria 		2 0 2 0.11 0 0
CUI: C2931042
Disease: Hawkinsinuria
Hawkinsinuria 		2 0 2 0.11 0 0
CUI: C1879362
Disease: Hypertyrosinemia
Hypertyrosinemia 		13 2 3 0.11 1 1.8E-02
CUI: C1848702
Disease: Elevated urinary delta-aminolevulinic acid
Elevated urinary delta-aminolevulinic acid 		3 0 2 0.11 0 0
CUI: C0268621
Disease: Hepatic methionine adenosyltransferase deficiency
Hepatic methionine adenosyltransferase deficiency 		16 0 3 9.7E-02 0 0
CUI: C4048705
Disease: Hypermethioninemia
Hypermethioninemia 		16 0 3 9.7E-02 0 0
CUI: C0268579
Disease: Propionic acidemia
Propionic acidemia 		17 0 3 9.4E-02 0 0
CUI: C3489576
Disease: Sexual Violence
Sexual Violence 		6 0 2 9.1E-02 0 0
CUI: C4023009
Disease: Constrictive median neuropathy
Constrictive median neuropathy 		8 0 2 8.3E-02 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 2 6.7E-02 0 0
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities 		16 0 2 6.2E-02 0 0
CUI: C0008625
Disease: Chromosome Aberrations
Chromosome Aberrations 		16 0 2 6.2E-02 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia 		1 0 1 5.6E-02 0 0
CUI: C0043325
Disease: Xanthomatosis
Xanthomatosis 		20 0 2 5.6E-02 0 0
CUI: C0085699
Disease: Cardiac cirrhosis
Cardiac cirrhosis 		1 0 1 5.6E-02 0 0
CUI: C0220982
Disease: Ketoacidosis
Ketoacidosis 		1 0 1 5.6E-02 0 0
CUI: C0268373
Disease: Congenital junctional epidermolysis bullosa-pyloric atresia syndrome
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome 		1 0 1 5.6E-02 0 0
CUI: C0268383
Disease: Familial amyloid polyneuropathy, type VI
Familial amyloid polyneuropathy, type VI 		1 0 1 5.6E-02 0 0
CUI: C0268385
Disease: Familial Amyloid Polyneuropathy, Jewish Type
Familial Amyloid Polyneuropathy, Jewish Type 		1 0 1 5.6E-02 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type 		1 0 1 5.6E-02 0 0