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3 entries on 1 page. Showing entries 1 - 3.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00486 255110 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 255110 0 0 CPT2 - -
00487 608836 CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 608836 0 0 CPT2 - -
00466 CPT II CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE;CPT2 600649 0 0 , CPT2 - -