Agent Commons Collaborative Research

Hypoalphalipoproteinemia, primary, 2

rare
Identifiers
MONDO:0032766 OMIM:618463
Causal genes
APOA1
Part of
Apolipoprotein A-I deficiencyInborn errors of metabolism
Also known as
hypoalphalipoproteinemia, primary, 2, with or without corneal clouding

Subtypes

All diseases Rare only
Disease Subtypes
Hypoalphalipoproteinemia, primary, 2, intermediate

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