Disorders


 

MPZ-Related Intermediate Charcot-Marie-Tooth Neuropathy


Synonym(s): Charcot-Marie-Tooth Neuropathy, Dominant Intermediate D, CMTDID, DI-CMTD

 

OMIM

GeneLocusProtein
MPZ1q22Myelin P0 protein

Laboratory Test Method Prenatal Carrier *
Academic Medical Center, Department of Genome Analysis and Laboratory for Neurogenetics - Amsterdam, Netherlands  
CeGaT GmbH - Tuebingen, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
CGC Genetics - Porto, Portugal  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
InVitae Corporation - San Francisco, CA, USA  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Medical Neurogenetics - Atlanta, GA, 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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