Disorders


 

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type


 

OMIM

GeneLocusProtein
DDR21q12-q23Discoidin domain-containing receptor 2

Laboratory Test Method Prenatal Carrier *
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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