Orphanet: Diagnostik des familiären Hyperaldosteronismus Typ 1 CYP11B1 Gen: Sequenzierung
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Diagnosis of familial hyperaldosteronism type 1 (CYP11B1 gene: sequencing)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 07/11/2014
  • Prnatal-Medizin Mnchen, Frauenrzte und Humangenetiker, Labor fr molekulare Genetik
  • Prnatal-Medizin Mnchen MVZ GmbH
  • Aiblingerstr. 8
  • 80639 MNCHEN
  • GERMANY
  • Director of laboratory : Dr Christoph BAGOWSKI
  • More information
  • Phone : 49 (0)89 1307 44 0
  • Additional Phone : -
  • Fax : 49 (0)89 1307 44 99
  • Website
  • Contact
Last update: November 2014

Responsible of diagnostic test

Purpose(s)

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) (1)

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.