Phenotype #0000207933

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00271323
Associated disease	EVR;FEVR
Phenotype details	unilateral congenital visual loss (HP:0030553), persistent hyperplasia primary vitreous (HP:0007968)
Diagnosis/Initial	-
Inheritance	Familial
Diagnosis/Definite	persistent hyperplasia primary vitreous
Age/Examination	19y (19 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Jasmine Chen
Database submission license	No license selected
Created by	Jasmine Chen
Date created	2019-12-18 00:48:22 +01:00 (CET)
Date last edited	2020-01-10 09:43:05 +01:00 (CET)

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