| 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 International |
| 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) |