systemic primary carnitine deficiency (Q3358135)
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amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy
- CTD, SPCD
- systemic primary carnitine deficiency disease
- carnitine transporter deficiency
- carnitine uptake defect
- deficiency of plasma-membrane carnitine transporter
- primary carnitine deficiency
- renal carnitine transport defect (disorder)
- renal carnitine transport defect
- Carnitine Transporter, Plasma-Membrane, Deficiency of
- CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP
- CARNITINE DEFICIENCY, SYSTEMIC PRIMARY
- CDSP
- Carnitine Deficiency, Systemic, Due to Defect 1N Renal Reabsorption of Carnitine
- Carnitine uptake deficiency
- Carnitine Deficiency, Primary
- Systemic Carnitine Deficiency
- Carnitine transporter defect
- SPCD
- CUD
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | systemic primary carnitine deficiency |
amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy |
|
Statements
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277.82
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Identifiers
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Sitelinks
Wikipedia(8 entries)
- arwiki عوز الكارنيتين الأساسي الجهازي
- bswiki Primarna deficijencija karnitina
- dawiki Karnitintransportørdefekt
- enwiki Systemic primary carnitine deficiency
- fowiki CTD
- nowiki Karnitintransportørdefekt
- svwiki Primär karnitinbrist
- zhwiki 卡尼丁缺乏症