Phenotype #0000067381

Individual ID 00087855
Associated disease LCA
Phenotype details Nystagmus; poor vision to cf ou; disc hyperemia and temporal pallor; vessels mildlyattenuated; bone spicules in midperiphery; ct normal; ekg normal; erg nonrecordable
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset ?
Phenotype/Onset Nystagmus
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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