Phenotype #0000174246

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00233811
Associated disease	?
Diagnosis/Initial	central choroidal sclerosis
Diagnosis/Definite	-
Phenotype details	visual acuity now R-counting vingers L-counting vingers; central scotoma (HP:0000603); mild central vision defect
Inheritance	Familial, autosomal recessive
Age/Examination	90y (90 years)
Age/Diagnosis	20y
Age/Onset	-
Phenotype/Onset	-
Protein	-
Tumor/MSI	-
Diagnosis/Criteria	-
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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