Peroxisomal acyl-CoA oxidase deficiency (Q88705): Difference between revisions
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Revision as of 15:05, 15 August 2026
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 |
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| 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. |
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CID11:ID_927825451
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dki-india-ID_927825451
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