Phenotype #0000174253

Individual ID 00233821
Associated disease STGD
Phenotype details visual acuity now R-20/200 L-20/50; central scotoma (HP:0000603); severe central vision defect; ERG rod-dec/cone-normal
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD-1
Age/Examination 62y (62 years)
Age/Diagnosis 39y
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Terry-Lynn Young
Database submission license No license selected
Created by Jim Houston
Date created 2019-03-20 11:55:21 +01:00 (CET)
Date last edited N/A

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