Phenotype #0000067421

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00087895
Associated disease	LCA15
Phenotype details	Congenital nystagmus, no or verypoor ocular pursuit, digito-ocular signs of franceschetti attesting of profoundly impaired vision, and no recordableerg since birth or the first months of life.
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Raheel Qamar
Database submission license	No license selected
Created by	Raheel Qamar
Date created	2012-09-06 09:49:02 +02:00 (CEST)
Date last edited	N/A

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