Phenotype #0000174548

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00234127
Associated disease	OI
Phenotype details	-
Diagnosis/Initial	osteogenesis imperfecta
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	OI-1
Age/Examination	21y (21 years)
Age/Onset	-
Phenotype/Onset	-
Protein	no collagen screen performed
Owner name	Global Variome, with Curator vacancy
Database submission license
Created by	Global Variome, with Curator vacancy
Date created	2019-01-13 12:23:00 +01:00 (CET)
Date last edited	N/A

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