Phenotype #0000174270

Individual ID 00233847
Associated disease STGD
Phenotype details visual acuity now R-20/400 L-20/200; central scotoma (HP:0000603); mild central vision defect; ERG rod-normal/cone-normal
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD-1
Age/Examination 56y (56 years)
Age/Diagnosis 26y
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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