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childhood hypophosphatasia

MeSH: C562440ORPHA: 247667

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Classification & Codes

Overview

hypophosphatasia that has material basis in an autosomal recessive mutation of ALPL on chromosome 1p36.12

Available Treatments (0)

No treatments linked yet

Clinical trials or compassionate use may be available — consult a specialist.

Classification & Codes

MeSH Code

C562440

Orphanet Code

ORPHA:247667
childhood hypophosphatasia
MeSHC562440
OrphanetORPHA:247667
Treatments0 drug(s)
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO