Phenotype #0000301989

Individual ID 00409875
Associated disease -
Phenotype details no electroretinogram responses at age 15; currently, no central vision
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite early onset retinal dystrophy
Age/Examination 25y (25 years)
Age/Diagnosis 3y
Age/Onset -
Phenotype/Onset nystagmus
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Anna Tracewska
Date created 2022-05-13 11:25:44 +02:00 (CEST)
Date last edited N/A

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