Human Disease and Mouse Model Detail
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Human Disease
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Carnitine Palmitoyltransferase II Deficiency, Infantile
OMIM ID: 600649
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Synonyms
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Carnitine Palmitoyltransferase II Deficiency with Hypoketotic Hypoglycemia;
Carnitine Palmitoyltransferase II Deficiency, Hepatocardiomuscular;
CPT2 Deficiency, Infantile;
CPT II Deficiency, Hepatic
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Cpt2
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CPT2*
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1:1 Homology
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Analysis Tools