Carnitine palmitoyltransferase II deficiency, neonatal form (Q104472): Difference between revisions
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Revision as of 10:19, 17 August 2026
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.
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| default for all languages | ID_1280842213 |
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| 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. |
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CID11:ID_1280842213
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dki-india-ID_1280842213
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