Phenotype #0000027067

Individual ID 00033638
Associated disease STGD
Phenotype details Stargardt disease, severe; severe cone-rod dystrophy; y37, visual acuity OD: 20/400, OS: 20/400. y32: Severe chorioretinal atrophy, macula up to periphery most affected
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination >07y (later than 7 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Miriam Bauwens
Database submission license No license selected
Created by Miriam Bauwens
Date created 2014-10-11 14:12:32 +02:00 (CEST)
Date last edited 2016-07-15 09:36:40 +02:00 (CEST)

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