Phenotype #0000157446

Individual ID 00208837
Associated disease -
Phenotype details 20/60 OD, 20/70 OS, nyctalopia, no nystagmus, bony spicules, flat ERG
Diagnosis/Initial Early onset retinal dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 15y (15 years)
Age/Diagnosis -
Age/Onset 00y18m
Phenotype/Onset -
Protein WBaileyGlen
Owner name Bailey Glen
Database submission license No license selected
Created by Bailey Glen
Date created 2018-12-17 20:25:33 +01:00 (CET)
Date last edited 2019-03-03 11:47:38 +01:00 (CET)

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