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Entry | Name | Description | Category | Pathway | Gene |
---|---|---|---|---|---|
H00392 |
VLCAD deficiency Very long-chain acyl-CoA dehydrogenase deficiency |
Very long chain acyl-coA dehydrogenase (VLCAD) deficiency is an autosomal recessive inborn error of fatty acid oxidation. Three phenotypes of VLCAD deficiency have been identified; an early onset, insidious ... | Inherited metabolic disorder | ACADVL [HSA:37] [KO:K09479] | |
H00525 | Disorders of mitochondrial fatty-acid oxidation | Disorders of mitochondrial fatty-acid oxidation are a group of rare inherited conditions that lead to accumulation of fatty acids and decreases in cell energy metabolism due to enzyme or transporter defects ... | Inherited metabolic disorder |
(MCAD) ACADM [HSA:34] [KO:K00249] (SCAD) ACADS [HSA:35] [KO:K00248] (VLCAD) ACADVL [HSA:37] [KO:K09479] (MTP) HADHA [HSA:3030] [KO:K07515] (MTP) HADHB [HSA:3032] [KO:K07509] (CPT I) CPT1A [HSA:1374] [KO:K08765] (CPT II) CPT2 [HSA:1376] [KO:K08766] (CACT) SLC25A20 [HSA:788] [KO:K15109] (CDSP) SLC22A5 [HSA:6584] [KO:K08202] (HAD) HADH [HSA:3033] [KO:K00022] (DECR) NADK2 [HSA:133686] [KO:K00858] (ACAD9) ACAD9 [HSA:28976] [KO:K15980] (ECHS1) ECHS1 [HSA:1892] [KO:K07511] |
[ KEGG | DISEASE | DRUG | MEDICUS ] |