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: C0040038
Disease: Thromboembolism
Thromboembolism 		25 0 3 4.5E-02 0 0
CUI: C0268611
Disease: Arakawa syndrome 2
Arakawa syndrome 2 		2 0 2 4.5E-02 0 0
CUI: C0342720
Disease: Adenosylcobalamin synthesis defect
Adenosylcobalamin synthesis defect 		2 0 2 4.5E-02 0 0
CUI: C1272348
Disease: Disorder of vitamin B12
Disorder of vitamin B12 		2 0 2 4.5E-02 0 0
CUI: C1848561
Disease: Methylmalonic acidemia with homocystinuria
Methylmalonic acidemia with homocystinuria 		2 58 2 4.5E-02 1 1.1E-02
CUI: C1855102
Disease: Methylmalonic aciduria cblB type
Methylmalonic aciduria cblB type 		2 27 2 4.5E-02 4 6.9E-02
CUI: C1855128
Disease: Methylcobalamin Deficiency, CblG Type
Methylcobalamin Deficiency, CblG Type 		2 0 2 4.5E-02 0 0
CUI: C3711369
Disease: Succinate-Coa Ligase Deficiency
Succinate-Coa Ligase Deficiency 		2 0 2 4.5E-02 0 0
CUI: C4693974
Disease: METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC 		2 0 2 4.5E-02 0 0
CUI: C0162275
Disease: Ketonuria
Ketonuria 		26 0 3 4.5E-02 0 0
CUI: C0342704
Disease: Deficiency of Cobalamin G
Deficiency of Cobalamin G 		3 0 2 4.4E-02 0 0
CUI: C0348484
Disease: Other disorders of branched-chain amino-acid metabolism
Other disorders of branched-chain amino-acid metabolism 		3 0 2 4.4E-02 0 0
CUI: C1855114
Disease: Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency 		3 169 2 4.4E-02 20 0.11
CUI: C3811915
Disease: SUCLA2
SUCLA2 		3 0 2 4.4E-02 0 0
CUI: C0002992
Disease: Angiomatosis
Angiomatosis 		4 0 2 4.3E-02 0 0
CUI: C0751316
Disease: Acquired Meningomyelocele
Acquired Meningomyelocele 		4 0 2 4.3E-02 0 0
CUI: C1298680
Disease: Occlusive stroke
Occlusive stroke 		4 0 2 4.3E-02 0 0
CUI: C3502298
Disease: Lactic Acidosis, Fatal Infantile
Lactic Acidosis, Fatal Infantile 		4 0 2 4.3E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 5 4.3E-02 0 0
CUI: C0086664
Disease: Myelocele
Myelocele 		5 0 2 4.3E-02 0 0
CUI: C0158629
Disease: Congenital anomaly of aortic arch
Congenital anomaly of aortic arch 		5 0 2 4.3E-02 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 3 4.2E-02 0 0
CUI: C0268464
Disease: Transient hyperphenylalaninemia
Transient hyperphenylalaninemia 		6 0 2 4.2E-02 0 0
CUI: C0268465
Disease: Phenylketonuria II
Phenylketonuria II 		6 0 2 4.2E-02 0 0
CUI: C0393698
Disease: Cryptogenic Infantile Spasms
Cryptogenic Infantile Spasms 		8 0 2 4.0E-02 0 0