Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal CPT2 disease C1833518 GeneticVariation 0.7 disgenet
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal CPT2 disease C1833518 Biomarker 0.7 disgenet
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal CPT2 disease C1833518 GermlineCausalMutation 0.7 disgenet
Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal CPT2 disease C1833518 CausalMutation 0.7 disgenet
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