Carnitine palmitoyltransferase 2 deficiency, lethal neonatal

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CPT II deficiency, lethal neonatal
MONDO_0012136
CPT2 Unknown
15622536 11994355 10873395 23911907 23184072 24843804 21913903 27604308 24816252 8651281 1528846
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Carnitine palmitoyltransferase 2 deficiency, lethal neonatal.
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Carnitine palmitoyltransferase 2 deficiency, myopathic, stress-induced 1 shared geneCPT2 Related via 1 shared gene including CPT2. Carnitine palmitoyltransferase 2 deficiency, infantile 1 shared geneCPT2 Related via 1 shared gene including CPT2. Carnitine palmitoyltransferase deficiency 1 shared geneCPT2 Related via 1 shared gene including CPT2. Brain disease 1 shared geneCPT2 Related via 1 shared gene including CPT2. Congenital neurologic anomalies 1 shared geneCPT2 Related via 1 shared gene including CPT2.