glutaric aciduria type 1 (Q2140501)
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Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder
- glutaryl-CoA dehydrogenase deficiency
- GA1
- glutaric acidemia type 1
- GCDHD
- GLUTARIC ACIDEMIA I
- Glutaryl-coenzyme A dehydrogenase deficiency
- Glutaric Aciduria 1
- Ga 1
- Glutaric Aciduria, Type 1
- Glutaric aciduria type 1
- glutaric acidemia I
- glutaric aciduria type I
- glutaric aciduria 1
- glutaryl-coenzyme A dehydrogenase deficiency
- glutaric academia type 1
- glutaryl-coA dehydrogenase deficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | glutaric aciduria type 1 |
Glutaryl-CoA dehydrogenase (GCDH) deficiency (GDD) is an autosomal recessive neurometabolic disorder clinically characterized by encephalopathic crises resulting in striatal injury and a severe dystonic dyskinetic movement disorder |
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17 May 2019
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270.7
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C99101
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Glutaric aciduria type 1
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Identifiers
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Wikipedia(11 entries)
- arwiki ارتفاع حمض الغلوتاريك في الدم من النوع الأول
- bswiki Glutarna acidemija tip 1
- dewiki Glutarazidurie
- elwiki Γλουταρική οξυουρία τύπου 1
- enwiki Glutaric aciduria type 1
- eswiki Aciduria glutárica tipo I
- fawiki گلوتاریک اسیدوری نوع یک
- mkwiki Глутарна ацидурија тип 1
- nlwiki Glutaaracidurie type 1
- plwiki Acyduria glutarowa typu I
- svwiki Glutarsyreuri typ 1
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Multilingual sites(1 entry)
- commonswiki Category:Glutaric aciduria type 1