Disorders


 

Syndromic Microphthalmia 9


Synonym(s): Matthew-Wood Syndrome, MCOPS9, Spear Syndrome

 

OMIM

GeneLocusProtein
STRA615q24.1Stimulated by retinoic acid gene 6 protein homolog

Laboratory Test Method Prenatal Carrier *
GeneDx - Gaithersburg, MD, USA  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  

* 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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