Phenotype #0000026857

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00033428
Associated disease	LCA
Phenotype details	Nystagmus;moderate pigmentry retionpathy;maculopathy atrophy; drusen; presence of white retinal dots; posterior subcapsular cataract; moderate myopia; Onset Poor vision, nystagmus
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	17y (17 years)
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Raheel Qamar
Database submission license	No license selected
Created by	Raheel Qamar
Date created	2012-10-12 13:26:32 +02:00 (CEST)
Date last edited	N/A

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