Phenotype #0000242491

Individual ID 00321052
Associated disease OI
Phenotype details Osteogenesis imperfecta type 4, subtype B,
Diagnosis/Initial -
Inheritance -
Diagnosis/Definite -
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Katarina Lindahl
Database submission license No license selected
Created by Katarina Lindahl
Date created 2014-12-05 13:29:50 +01:00 (CET)
Date last edited 2015-08-07 14:49:10 +02:00 (CEST)

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