Global Variome shared LOVD

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

Phenotype #0000227908 Individual ID 00289016 Associated disease - Phenotype details RP, night blindness, pericentral field loss Diagnosis/Initial retinitis pigmentosa Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 11y (11 years) Age/Diagnosis - Age/Onset 10y Phenotype/Onset - Protein - Owner name Sandro Banfi Database submission license No license selected Created by Johan den Dunnen Date created 2020-05-03 16:46:49 +02:00 (CEST) Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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