Orphanet: Biochemical diagnosis of Hypophosphatasia Analyte: Phosphoethanolamine

Search for a diagnostic test

* (*) mandatory field

Biochemical diagnosis of Hypophosphatasia (Analyte: Phosphoethanolamine)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 11/08/2009
  • Department of Paediatric Biochemistry
  • Royal Hospital for Sick Children
  • 9 Sciennes Road
  • Director of laboratory : Dr Leigh CAMPBELL
  • More information
  • Phone : 44 (0)131 536 0415
  • Additional Phone : -
  • Fax : 44 (0)131 536 0410
Last update: August 2009

Responsible of diagnostic test


Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay

List of diseases and genes

List of diseases tested (1)
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.