Global Variome shared LOVD

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Phenotype #0000268212 Individual ID 00372936 Associated disease OI Phenotype details 3 fractures; no blue sclerae; no dentinogenesis imperfecta; no hearing loss; not able to walk independently; no ptosis Diagnosis/Initial osteogenesis imperfecta Inheritance Familial, autosomal recessive Diagnosis/Definite OI6 Age/Examination - Age/Onset - Phenotype/Onset - Protein - Owner name Xiuli Zhao Database submission license No license selected Created by Xiuli Zhao Date created 2018-09-25 13:41:22 +02:00 (CEST) Date last edited 2026-01-12 09:09:46 +01:00 (CET)

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