Phenotype #0000292471

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Katarina Pelin, Vilma-Lotta Lehtokari, and Johan den Dunnen

Individual ID	00399354
Associated disease	FVH2
Phenotype details	secondary nystagmus and low vision
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	FVH2
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Yonatan Perez
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2013-12-24 22:34:45 +01:00 (CET)
Date last edited	N/A

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