Phenotype #0000221714

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00287981
Associated disease	neuropathy, optic
Phenotype details	-
Diagnosis/Initial	-
Diagnosis/Definite	-
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Khadidja Guehlouz
Database submission license	No license selected
Created by	Khadidja Guehlouz
Date created	2020-02-14 20:18:44 +01:00 (CET)
Date last edited	2020-06-20 11:22:35 +02:00 (CEST)

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