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GTR Home > Conditions/Phenotypes > Hypoalphalipoproteinemia, primary, 1

Hypoalphalipoproteinemia, primary, 1

Synonyms
ABCA1-Associated Familial High Density Lipoprotein Deficiency; ABCA1-Related Familial High Density Lipoprotein Deficiency

Summary

Any ypoalphalipoproteinemia in which the cause of the disease is a mutation in the ABCA1 gene. [from MONDO]

Available tests

26 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (26 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ABC-1, ABC1, CERP, HDLCQTL13, HDLDT1, HPALP1, TGD, ABCA1
    Summary: ATP binding cassette subfamily A member 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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