Phenotype #0000268092

Individual ID 00372815
Associated disease OI
Phenotype details The authors were contacted for further clarification of the OI type. They stated that this patient if classified according to pathogenic genes, is likely to have the type XV. Also, they stated that the patient could also be classified as type 4 according to the 5 types of OI (Bonafe et al., 2015, PMID: 26394607).
Diagnosis/Initial OI
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Raymond Dalgleish
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Raymond Dalgleish
Date created 2019-08-16 11:25:51 +02:00 (CEST)
Date last edited 2021-05-16 14:29:51 +02:00 (CEST)

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