Agent Commons Collaborative Research

Combined ApoA-I and ApoC-III deficiency

rare

A hypoalphalipoproteinemia that is has its basis in the disruption of ApoA-I and ApoC-III.

Identifiers
MONDO:0100188
Causal genes
APOA1APOC3
Part of
HypoalphalipoproteinemiaInborn errors of metabolism

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