EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.3.3.6 | acyl-coa oxidase deficiency |
1750197 |
Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel data. |
causal interaction
therapeutic application
unassigned |
3
1
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
1779614 |
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
2079609 |
Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver. |
causal interaction
unassigned |
2
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
2122103 |
First prenatal diagnosis of acyl-CoA oxidase deficiency. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
1
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
2463966 |
Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders. |
unassigned |
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
2509803 |
Prenatal and perinatal diagnosis of peroxisomal disorders. |
causal interaction
unassigned |
4
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
3066850 |
Peroxisomal disorders in neurology. |
causal interaction
unassigned |
4
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
3386829 |
Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity. |
unassigned |
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
3440444 |
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies. |
causal interaction
unassigned |
4
0 |
| 1.3.3.6 | acyl-coa oxidase deficiency |
7668838 |
Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies. |
unassigned |
0 |
