Phenotype #0000092983

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Gert Matthijs

Individual ID	00117513
Associated disease	MYP21
Phenotype details	see paper; …, high myopia
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Gerard C.P. Schaafsma
Date created	2011-07-14 16:21:46 +02:00 (CEST)
Date last edited	N/A

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