Phenotype #0000174267

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00233842
Associated disease	STGD
Phenotype details	visual acuity now R-20/80 L-counting vingers; central scotoma (HP:0000603); severe central vision defect; ERG rod-slight dec/cone-slight dec
Diagnosis/Initial	Stargardt disease
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	STGD-1
Age/Examination	66y (66 years)
Age/Diagnosis	47y
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Terry-Lynn Young
Database submission license	No license selected
Created by	Jim Houston
Date created	2019-03-20 11:55:21 +01:00 (CET)
Date last edited	N/A

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