Definition

A familial chylomicronemia syndrome characterized by onset in adolescence or adulthood of hypertriglyceridemia and fasting chylomicronemia that has_material_basis_in homozygous or compound heterozygous mutation in the APOC2 gene on chromosome 19q13.32.

[1]

Synonyms

C-II anapolipoproteinemia
familial apoC-II deficiency

Cross References

Parent Terms

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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familial apolipoprotein C-II deficiency

familial apolipoprotein C-II deficiency

Associated Genes

Associated Alleles

Associated Models