Phenotype #0000302272

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00410168
Associated disease	OI13
Phenotype details	Dentinogenesis imperfecta (HP:0000703), no Blue sclerae (-HP:0000592), no Hearing abnormality (-HP:0000364)
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	06y (6 years)
Age/Diagnosis	-
Age/Onset	03y
Phenotype/Onset	Bone fracture (HP:0020110)
Protein	-
Owner name	Thanakorn Theerapanon
Database submission license
Created by	Thanakorn Theerapanon
Date created	2022-05-19 14:47:47 +02:00 (CEST)
Date last edited	2022-05-20 15:29:46 +02:00 (CEST)

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