Orphanet: Diagnostik der Hypoalphalipoprotein�mie ABCA1 , APOA1 und LCAT Gen

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Diagnosis of hypoalphalipoproteinemia (ABCA1, APOA1, LCAT genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 22/11/2016
  • Phone : 49 (0)89 1307 44 0
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  • Fax : 49 (0)89 1307 44 99
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Last update: November 2016

Responsible of diagnostic test


Antenatal diagnosis
Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (3)

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.