Phenotype #0000268065

Individual ID 00372788
Associated disease OI
Phenotype details 5y-first fracture, 3 fractures; height Z -1.71; no scoliosis; blue sclerae; no dentinogenesis imperfecta; no hearing loss; able to walk; no ptosis
Diagnosis/Initial osteogenesis imperfecta
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Xiuli Zhao
Database submission license No license selected
Created by Xiuli Zhao
Date created 2018-09-26 08:32:59 +02:00 (CEST)
Date last edited 2026-01-12 09:34:08 +01:00 (CET)

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