Global Variome shared LOVD

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

Phenotype #0000274789 Individual ID 00380936 Associated disease LISX1;SCLH Phenotype details Double-Cortex syndrome with Seizure, Motor seizure, Myoclonic seizure Diagnosis/Initial - Inheritance Familial, X-linked Diagnosis/Definite 28y Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-08-24 12:32:55 +02:00 (CEST) Date last edited 2021-08-24 16:18:40 +02:00 (CEST)

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