Phenotype #0000220906

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00287171
Associated disease	neuropathy, optic
Phenotype details	Abnormal macular morphology (HP:0001103); Mycrocyst
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal dominant
Age/Examination	20y (20 years)
Age/Diagnosis	-
Age/Onset	03y
Phenotype/Onset	Progressive visual loss (HP:0000529)
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-14 11:06:59 +01:00 (CET)
Date last edited	2020-08-25 21:27:59 +02:00 (CEST)

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