Orphanet: Biochemical diagnosis of Hypophosphatasia Analyte: Phosphoethanolamine
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Biochemical diagnosis of Hypophosphatasia (Analyte: Phosphoethanolamine)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 23/07/2010
  • Biochemical Genetics Unit
  • Box 247, Department of Clinical Biochemistry and Immunology
  • Addenbrooke's Hospital
  • Hills Road
  • CAMBRIDGE CB2 0QQ
  • UNITED KINGDOM
  • Director of laboratory : Dr Jacqui CALVIN
  • More information
  • Phone : 44 (0)1223 245151
  • Additional Phone : -
  • Fax : 44 (0)1223 216 867
  • Website
Last update: July 2010

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Biochemical genetics
Analyte / Enzyme assay
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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.