Disorders

Hyperphosphatasia with Mental Retardation Syndrome 2

Synonym(s): HPMRS2

Gene	Locus	Protein
PIGO	9p13.2	GPI ethanolamine phosphate transferase 3

Laboratory	Test Method	Prenatal	Carrier *
Centogene AG, Rare Disease Company - Rostock, Germany
Charit Unversitaetsmedizin Berlin, Institute of Medical Genetics and Human Genetics - Berlin, Germany

^* 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.