Phenotype #0000327913

Individual ID 00438009
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details movement disorder; developmental epileptic encephalopathy; developmental delay; 2h-onset epilepsy; structural changes brain; 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 InternationalCreative Commons License
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.