Phenotype #0000092587

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	00117352
Associated disease	STL1
Phenotype details	myopia, retinal detachment
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Mouna Barat-Houari
Database submission license	No license selected
Created by	Mouna Barat-Houari
Date created	2017-08-21 15:51:32 +02:00 (CEST)
Date last edited	N/A

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