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Hyperammonaemia v1.13 CPT2 Arina Puzriakova Phenotypes for gene: CPT2 were changed from CPT deficiency, hepatic, type II 600649; CPT II deficiency, lethal neonatal 608836 to CPT II deficiency, infantile, OMIM:600649; CPT II deficiency, lethal neonatal, OMIM:608836
Hyperammonaemia CPT2 Sarah Leigh marked CPT2 as ready
Hyperammonaemia CPT2 Sarah Leigh commented on CPT2