Global Variome shared LOVD

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

Phenotype #0000327927 Individual ID 00438023 Associated disease ? Diagnosis/Initial - Diagnosis/Definite - Phenotype details neonatal onset movement disorder; movement disorder; epilepsy; developmental delay; <0d-onset epilepsy; structural changes brain, atrophy; hypotonia; no speech Inheritance Unknown Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Harald Mikkers Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-08-14 14:11:00 +02:00 (CEST) Date last edited N/A

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