Disorders


 

Mucopolysaccharidosis Type IX


Synonym(s): Hyaluronidase Deficiency, MPS IX, MPS9

 

OMIM

GeneLocusProtein
HYAL13p21.3-p21.2Hyaluronidase-1

Laboratory Test Method Prenatal Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
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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