Phenotype #0000067357

Individual ID 00087826
Associated disease LCA15
Phenotype details Congenital nystagmus,no or verypoor ocular pursuit,digito-ocular signs of franceschetti attesting of profoundly impaired vision,no recordable erg since birth or the first months of life
Diagnosis/Initial -
Inheritance Unknown
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 09:49:01 +02:00 (CEST)
Date last edited N/A

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