Phenotype #0000352339

Individual ID 00467132
Associated disease NDD
Diagnosis/Initial neurodevelopmental disorder
Diagnosis/Definite -
Phenotype details see paper; ..., plagiocephaly; seizures, focal-onset seizure; spasticity; autism; abnormal repetitive mannerisms; stereotypical hand wringing; no speech; global developmental delay; delayed gross motor development; dystonia; broad-based gait; inability to walk; failure to thrive; hypertonia
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-10-08 11:17:07 +02:00 (CEST)
Date last edited 2025-10-08 11:46:03 +02:00 (CEST)

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