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 26/09/2007
  • Department of Clinical Chemistry
  • B Floor, Orange Wing, Pathology Block
  • The Sheffield Children's Hospital
  • Western Bank
  • Director of laboratory : Dr James BONHAM
  • More information
  • Phone : 44 (0)114 271 7307
  • Additional Phone : -
  • Fax : 44 (0)114 270 6121
  • Website
Last update: September 2007

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.