Peroxisomal acyl-CoA oxidase deficiency (Q88705): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (3 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_927825451 | |||||||||||||||
| Property / Canary Token: dki-india-ID_927825451 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest 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 |
||
| 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
0 references
dki-india-ID_927825451
0 references
Concluído
0 references
13 August 2026
0 references
