Phenotype #0000130106

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00155750
Associated disease	STL
Phenotype details	HP:0004327 Abnormality of the vitreous humor HP:0000545 Myopia HP:0000110 Renal dysplasia
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	20y (20 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Thomas Nixon
Database submission license	No license selected
Created by	Thomas Nixon
Date created	2018-07-02 16:49:53 +02:00 (CEST)
Date last edited	2018-07-03 16:06:50 +02:00 (CEST)

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