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: C0268130
Disease: Hereditary orotic aciduria, type 1
Hereditary orotic aciduria, type 1 		3 0 3 0.17 0 0
CUI: C1839541
Disease: Episodic ammonia intoxication
Episodic ammonia intoxication 		4 0 3 0.16 0 0
CUI: C1839531
Disease: Protein avoidance
Protein avoidance 		5 0 3 0.15 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 3 0.14 0 0
CUI: C0268542
Disease: Ornithine carbamoyltransferase deficiency
Ornithine carbamoyltransferase deficiency 		17 0 4 0.13 0 0
CUI: C4082171
Disease: Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency
Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency 		2 0 2 0.11 0 0
CUI: C0270710
Disease: Bing-Neel syndrome
Bing-Neel syndrome 		3 0 2 0.11 0 0
CUI: C4085580
Disease: Carbamoyl Phosphate Synthase 1 Deficiency
Carbamoyl Phosphate Synthase 1 Deficiency 		3 0 2 0.11 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 3 0.10 0 0
CUI: C0410214
Disease: Myopathy with Abnormal Lipid Metabolism
Myopathy with Abnormal Lipid Metabolism 		4 0 2 1.0E-01 0 0
CUI: C4025095
Disease: Hypoargininemia
Hypoargininemia 		4 0 2 1.0E-01 0 0
CUI: C1839533
Disease: Hyperglutaminemia
Hyperglutaminemia 		5 0 2 9.5E-02 0 0
CUI: C0268128
Disease: Orotic aciduria
Orotic aciduria 		6 0 2 9.1E-02 0 0
CUI: C0268505
Disease: Ocular albinism, type II
Ocular albinism, type II 		7 0 2 8.7E-02 0 0
CUI: C0014534
Disease: Epididymitis
Epididymitis 		8 0 2 8.3E-02 0 0
CUI: C0162532
Disease: Variegate Porphyria
Variegate Porphyria 		21 0 3 8.3E-02 0 0
CUI: C0949116
Disease: Congenital hypoplastic anemia
Congenital hypoplastic anemia 		8 0 2 8.3E-02 0 0
CUI: C3672440
Disease: Bile duct hyperplasia
Bile duct hyperplasia 		9 0 2 8.0E-02 0 0
CUI: C0019188
Disease: Hepatitis, Animal
Hepatitis, Animal 		11 0 2 7.4E-02 0 0
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia 		11 0 2 7.4E-02 0 0
CUI: C0006114
Disease: Cerebral Edema
Cerebral Edema 		26 0 3 7.3E-02 0 0
CUI: C0043046
Disease: Wasting Syndrome
Wasting Syndrome 		26 0 3 7.3E-02 0 0
CUI: C0264393
Disease: Panacinar Emphysema
Panacinar Emphysema 		12 0 2 7.1E-02 0 0
CUI: C2350878
Disease: Focal Emphysema
Focal Emphysema 		12 0 2 7.1E-02 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 2 7.1E-02 0 0