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: C0027063
Disease: Myoclonic disorder
Myoclonic disorder 		1 0 1 1.7E-02 0 0
CUI: C0033247
Disease: Proctocolitis
Proctocolitis 		1 0 1 1.7E-02 0 0
CUI: C0239778
Disease: Green urine
Green urine 		1 0 1 1.7E-02 0 0
CUI: C0268152
Disease: Classical galactosemia, homozygous Duarte-type
Classical galactosemia, homozygous Duarte-type 		1 0 1 1.7E-02 0 0
CUI: C0270150
Disease: Perinatal respiratory failure
Perinatal respiratory failure 		1 0 1 1.7E-02 0 0
CUI: C0270975
Disease: Infantile encephalopathy AND lactic acidosis
Infantile encephalopathy AND lactic acidosis 		1 0 1 1.7E-02 0 0
CUI: C0342858
Disease: Homozygous acute intermittent porphyria
Homozygous acute intermittent porphyria 		1 0 1 1.7E-02 0 0
CUI: C0554980
Disease: Moody (finding)
Moody (finding) 		1 0 1 1.7E-02 0 0
CUI: C0853398
Disease: Endocarditis enterococcal
Endocarditis enterococcal 		1 0 1 1.7E-02 0 0
CUI: C1142277
Disease: Brown urine
Brown urine 		1 1 1 1.7E-02 1 0.20
CUI: C1261251
Disease: Agenesis of vagina
Agenesis of vagina 		1 0 1 1.7E-02 0 0
CUI: C1266156
Disease: Multicystic mesothelioma, benign
Multicystic mesothelioma, benign 		1 0 1 1.7E-02 0 0
CUI: C1268588
Disease: Porphyric polyneuropathy
Porphyric polyneuropathy 		1 0 1 1.7E-02 0 0
CUI: C1274925
Disease: Skin-ache syndrome
Skin-ache syndrome 		1 0 1 1.7E-02 0 0
CUI: C1275125
Disease: Inherited disorder of porphyrin metabolism
Inherited disorder of porphyrin metabolism 		1 0 1 1.7E-02 0 0
CUI: C1291329
Disease: Transaldolase Deficiency
Transaldolase Deficiency 		1 0 1 1.7E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 1.7E-02 0 0
CUI: C1655035
Disease: congenital muscle disorder
congenital muscle disorder 		1 0 1 1.7E-02 0 0
CUI: C1739147
Disease: Subacute necrotising encephalomyopathy
Subacute necrotising encephalomyopathy 		1 0 1 1.7E-02 0 0
CUI: C1855790
Disease: Hepatic glycogen storage
Hepatic glycogen storage 		1 0 1 1.7E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 1.7E-02 0 0
CUI: C1867969
Disease: Porphyria, Acute Intermittent, Nonerythroid Variant
Porphyria, Acute Intermittent, Nonerythroid Variant 		1 0 1 1.7E-02 0 0
CUI: C2584751
Disease: Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor 		1 0 1 1.7E-02 0 0
CUI: C2584777
Disease: Autoimmune thrombotic thrombocytopenic purpura
Autoimmune thrombotic thrombocytopenic purpura 		1 0 1 1.7E-02 0 0
CUI: C2931007
Disease: Congenital disorder of glycosylation type 1X
Congenital disorder of glycosylation type 1X 		1 0 1 1.7E-02 0 0