Global Variome shared LOVD

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Phenotype #0000268053 Individual ID 00372776 Associated disease OI Phenotype details see paper; ..., bone fragility, osteopenia, dentinogenesis imperfecta Diagnosis/Initial osteogenesis imperfecta Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Raymond Dalgleish Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Raymond Dalgleish Date created 2017-02-07 09:08:54 +01:00 (CET) Date last edited 2026-01-10 10:49:55 +01:00 (CET)

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