Phenotype #0000277522

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00383737
Associated disease	-
Phenotype details	RE retinal fold with peripheral chorioretinal atrophy and pigment LE focal chorioretinopathy Normal MRI brain
Diagnosis/Initial	Familial exudative vitreoretinopathy associated with microcephaly
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	14y (14 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-09-29 12:36:52 +02:00 (CEST)
Date last edited	N/A

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