Carnitine palmitoyltransferase II deficiency, neonatal form (Q104472)
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The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1280842213 |
||
| English | Carnitine palmitoyltransferase II deficiency, neonatal form |
The neonatal form of carnitine palmitoyltransferase II (CPT II) deficiency, an inherited disorder that affects mitochondrial oxidation of long chain fatty acids (LCFA), is the lethal form of the disease which presents with multisystem failure. |
Statements
CID11:ID_1280842213
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dki-india-ID_1280842213
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Concluído
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16 August 2026
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