Phenotype #0000026931

Individual ID 00033502
Associated disease LCA
Phenotype details Cataract; retinal degeneration; foveal depression; Onset Visual disturbance, nystagmus, visual acuity, nyctalopia
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 45y (45 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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