Disorders


 

Hyalinosis, Inherited Systemic


 

GeneReviewOMIM

GeneLocusProtein
ANTXR24q21.3Anthrax toxin receptor 2

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
University of Lausanne, Division of Molecular Pediatrics - Lausanne, Switzerland  

* 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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