Disorders


 

F5-Related Budd-Chiari Syndrome


 

OMIM

GeneLocusProtein
F51q23Coagulation factor V

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
• Targeted mutation analysis
 
GENETIX Centro de Investigación en Genética Humana y Reproductiva - Bogota, Colombia• Targeted mutation analysis
 
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany• Sequence analysis of the entire coding region
 

* 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...