Disorders


 

Cataract, Autosomal Dominant, Multiple Types 1


 

OMIM

GeneLocusProtein
BFSP23q22.1Phakinin

Laboratory Test Method Prenatal Carrier *
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Medgene, MedGene - Bratislava, Slovakia  
Praxis fuer Humangenetik Wien - Vienna, Austria  

* 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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