Carnitine palmitoyltransferase i deficiency, hepatic, type ia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CPT deficiency, hepatic, type IA
MONDO_0009705
CPT1A Unknown
27604308
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Carnitine palmitoyltransferase i deficiency, hepatic, type ia.
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Carnitine palmitoyltransferase deficiency 1 shared geneCPT1A Related via 1 shared gene including CPT1A. Fatty acid metabolism disorder 1 shared geneCPT1A Related via 1 shared gene including CPT1A. Vitiligo 1 shared geneCPT1A Related via 1 shared gene including CPT1A. Cataract 1 shared geneCPT1A Related via 1 shared gene including CPT1A. Kidney failure 1 shared geneCPT1A Related via 1 shared gene including CPT1A.