Phenotype #0000174247

Individual ID 00233812
Associated disease STGD
Phenotype details visual acuity now R-counting vingers 3 ft L- hand motion; central scotoma (HP:0000603); medium central vision defect
Diagnosis/Initial Stargardt disease
Inheritance Familial, autosomal recessive
Diagnosis/Definite STGD-1
Age/Examination 75y (75 years)
Age/Diagnosis 45y
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

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.