Disorders


 

Hyperaldosteronism, Familial, Type III


Synonym(s): Familial Hyperaldosteronism Type 3, Familial Hyperaldosteronism Type III, FH III

 

OMIM

GeneLocusProtein
KCNJ511q24G protein-activated inward rectifier potassium channel 4

Laboratory Test Method Prenatal Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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