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: C1864399
Disease: Peroxisome Biogenesis Disorder, Complementation Group 7
Peroxisome Biogenesis Disorder, Complementation Group 7 		2 0 1 0.50 0 0
CUI: C2364135
Disease: Discomfort
Discomfort 		2 0 1 0.50 0 0
CUI: C0268600
Disease: 3-methylcrotonyl CoA carboxylase 1 deficiency
3-methylcrotonyl CoA carboxylase 1 deficiency 		5 0 1 0.20 0 0
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia 		5 0 1 0.20 0 0
CUI: C4551505
Disease: Methylcrotonyl-CoA carboxylase deficiency
Methylcrotonyl-CoA carboxylase deficiency 		5 0 1 0.20 0 0
CUI: C0241775
Disease: Organic aciduria
Organic aciduria 		12 0 1 8.3E-02 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 1 7.1E-02 0 0
CUI: C0268579
Disease: Propionic acidemia
Propionic acidemia 		17 0 1 5.9E-02 0 0
CUI: C4022001
Disease: Abnormality of the cerebral vasculature
Abnormality of the cerebral vasculature 		18 0 1 5.6E-02 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria 		26 0 1 3.8E-02 0 0
CUI: C0151818
Disease: Opisthotonus
Opisthotonus 		32 0 1 3.1E-02 0 0
CUI: C0036508
Disease: Seborrheic dermatitis
Seborrheic dermatitis 		39 0 1 2.6E-02 0 0
CUI: C0221765
Disease: Chronic schizophrenia
Chronic schizophrenia 		48 0 1 2.1E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 1 1.3E-02 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 1.2E-02 0 0
CUI: C1867873
Disease: Failure to thrive in infancy
Failure to thrive in infancy 		97 0 1 1.0E-02 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 1.0E-02 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		102 0 1 9.8E-03 0 0
CUI: C0022638
Disease: Ketosis
Ketosis 		119 0 1 8.4E-03 0 0
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		126 0 1 7.9E-03 0 0
CUI: C0023380
Disease: Lethargy
Lethargy 		160 0 1 6.3E-03 0 0
CUI: C0042963
Disease: Vomiting
Vomiting 		303 0 1 3.3E-03 0 0
CUI: C0541794
Disease: Skeletal muscle atrophy
Skeletal muscle atrophy 		306 0 1 3.3E-03 0 0
CUI: C0035229
Disease: Respiratory Insufficiency
Respiratory Insufficiency 		315 0 1 3.2E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 0 1 2.8E-03 0 0