Phenotype #0000026927

Individual ID 00033498
Associated disease LCA
Phenotype details Bone specule like changes; Bull's eye appearence; Atrophic macular lesions; drusion like deposits;  Oculodigital Phenomena; Onset Visual Loss, Severe pigmentary retinopathy, Atrophy of retinal pigment, mottling of hypopigmentation.
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
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 2012-10-12 13:26:32 +02:00 (CEST)
Date last edited N/A

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