Disorders


 

Charcot-Marie-Tooth Neuropathy Type 2N


Synonym(s): CMT2N

 

OMIM

GeneLocusProtein
AARS16q22 

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
InVitae Corporation - San Francisco, CA, USA  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany  

* 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.

Loading...