Global Variome shared LOVD

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Phenotype #0000243080 Individual ID 00324553 Associated disease HPP Diagnosis/Initial hypophosphatasia Diagnosis/Definite - Phenotype details prenatal, asymptomatic, repeatedly low serum alkaline phosphatase, no hypophosphatasia clinical symptom Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2020-12-18 17:55:13 +01:00 (CET) Date last edited 2020-12-18 18:01:06 +01:00 (CET)

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