All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01955 - carnitine palmitoyltransferase II deficiency, late-onset 255110 - - - CPT2 - -
02308 - carnitine palmitoyltransferase II deficiency, infantile 600649 - - - CPT2 - -
02798 - carnitine palmitoyltransferase II deficiency, lethal neonatal 608836 - - - CPT2 - -
03583 - Encephalopathy, acute, infection-induced, 4, susceptibility to 614212 - - - CPT2 - -
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