peroxisomal acyl-CoA oxidase deficiency (Q18553481)
Jump to navigation
Jump to search
peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy
- Peroxisomal acyl-coenzyme A oxidase
- Pseudoneonatal Adrenoleukodystrophy
- Straight-Chain Acyl-Coa Oxidase Deficiency
- Pseudoadrenoleukodystrophy
- Pseudo-neonatal adrenoleukodystrophy
- Pseudo-NALD
- PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY
- Acyl-CoA oxidase deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | peroxisomal acyl-CoA oxidase deficiency |
peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy |
|
Statements
1 reference
1 reference
1 reference
4 references
255.41
1 reference
C170437
0 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(1 entry)
- enwiki Acyl-CoA oxidase deficiency