Global Variome shared LOVD

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

Phenotype #0000185625 Individual ID 00245757 Associated disease - Phenotype details Persistent microhaematuria, proteinuria, astigmatism and myopia. Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Alessandra Renieri Database submission license No license selected Created by Alessandra Renieri Date created 2019-07-08 09:59:35 +02:00 (CEST) Date last edited 2019-07-12 09:40:23 +02:00 (CEST)

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.