Orphanet: Diagnóstico del hiperaldosteronismo familiar tipo I gen híbrido de duplicación CYP11B1B2

Search for a diagnostic test

* (*) mandatory field

Diagnosis of familial hyperaldosteronism type 1 (CYP11B1/B2 genes, duplication hybrid gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 17/01/2017
  • Laboratorio de Diagnstico Molecular
  • Hospital Materno Infantil Gregorio Maran
  • Calle Maiquez, 9
  • 28009 MADRID
  • Director of laboratory : -
  • More information
  • Phone : 34 915 29 00 87
  • Additional Phone : -
  • Fax : 34 915 86 80 18
  • Website
Last update: January 2017

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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.