[ Network menu | Network entry | Edit Network | Help ]

ENTRY	nt06024
Name	Valine, leucine and isoleucine degradation
Category	Congenital disorders of metabolism
Pathway	hsa00280
Module	hsa_M00036 hsa_M00741
Display	drug-target relation   disease type

N00832        MSUD (type Ia)     MSUD (type Ib)     MSUD (type II)     MSUD (type III)   N00851        Isovaleric acidemia     3-Methylcrotonylglycinuria     3-Methylcrotonylglycinuria     MGCA1     HL deficiency   N00852        IBD deficiency     Methacrylic aciduria     MMSDH deficiency   N00856        SBCAD deficiency     MHBD deficiency   N00842        Propionic acidemia     Propionic acidemia     MCE deficiency     MMA mut type