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Summary Literature (0)
MIM:207750 - APOLIPOPROTEIN C-II DEFICIENCY

Xenbase Genes: apoc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008810 - nasopalatine nerve
MONDO:0018637 - familial chylomicronemia syndrome

Disease Ontology (DO):
DOID:0111418 - familial apolipoprotein C-II deficiency