Phenotype #0000222591

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00288895
Associated disease	neuropathy, optic
Phenotype details	Amblyopia (HP:0000646); Peripheral neuropathy (HP:0009830); Hypertension (HP:0000822)
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal recessive
Age/Examination	50y (50 years)
Age/Diagnosis	-
Age/Onset	43y
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-24 20:37:42 +01:00 (CET)
Date last edited	2020-06-20 13:30:22 +02:00 (CEST)

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