Disorders


 

Complement Component C2 Deficiency


Synonym(s): C2 Deficiency, C2D

 

OMIM

GeneLocusProtein
C26p21.3Complement C2

Laboratory Test Method Prenatal Carrier *
Centre for Cardiovascular Surgery and Transplantation, Molecular Genetics Laboratory - Brno, Czech Republic• Targeted mutation analysis
 
National Jewish Health, Advanced Diagnostic Laboratories (ADx) - Denver, CO, USA• Targeted mutation analysis
 

* 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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