Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000257298 Individual ID 00361902 Associated disease USH2C Phenotype details Deafness, blurring of vision, generalised hypopigmentation, light coloured iris Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Anju Shukla Database submission license No license selected Created by Anju Shukla Date created 2021-04-12 06:39:21 +02:00 (CEST) Date last edited 2021-04-12 14:20:07 +02:00 (CEST)

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