Global Variome shared LOVD

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

Phenotype #0000081291 Individual ID 00103214 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details see paper, epilepsy, hearing loss, developmental delay Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset <00y01m Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Sander Pajusalu Database submission license Creative Commons Attribution 4.0 International Created by Sander Pajusalu Date created 2017-04-09 20:28:48 +02:00 (CEST) Date last edited 2017-04-11 15:13:50 +02:00 (CEST)

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