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Entry | Name | Description | Category | Pathway | Gene |
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H02711 | Acetyl-CoA carboxylase-alpha deficiency | Acetyl-CoA carboxylase-alpha deficiency (ACACAD) is a rare autosomal recessive inborn error of metabolism caused by mutations in ACACA. ACACAD is characterized by hypotonia, motor and intellectual developmental ... | Inherited metabolic disorder | ACACA [HSA:31] [KO:K11262] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |