Peroxisomal acyl-CoA oxidase deficiency (Q88705)
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Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterised by hypotonia and seizures in the neonatal period and neurological regression in early infancy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_927825451 |
||
| English | Peroxisomal acyl-CoA oxidase deficiency |
Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterised by hypotonia and seizures in the neonatal period and neurological regression in early infancy. |
Statements
CID11:ID_927825451
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dki-india-ID_927825451
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