Carnitine palmitoyltransferase 2 deficiency, myopathic, stress-induced

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Subtype of: Carnitine palmitoyltransferase deficiency
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Carnitine palmitoyltransferase 2 deficiency, myopathic, stress-induced
MONDO_0009704
CPT2 Unknown
10090476 11477613 14605500 14615409 1528846 15489334 15622536 24780397 7711730 8358442 8651281 9600456 9758712
Open Targets
CPT II deficiency, myopathic, stress-induced
MONDO_0009704
CPT2 Unknown
15622536 11994355 10873395 23911907 23184072 24843804 21913903 27604308 24816252
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Carnitine palmitoyltransferase 2 deficiency, myopathic, stress-induced.
5 View disease cluster →
Carnitine palmitoyltransferase 2 deficiency, infantile 1 shared geneCPT2 Related via 1 shared gene including CPT2. Carnitine palmitoyltransferase 2 deficiency, lethal neonatal 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.