Phenotype #0000242121

Individual ID 00320076
Associated disease NYS1
Phenotype details Congenital nystagmus, possible foveal hypoplasia
Diagnosis/Initial 1y
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2020-11-23 13:28:57 +01:00 (CET)
Date last edited 2020-12-09 10:32:54 +01:00 (CET)

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