| Individual ID |
00313959 |
| Associated disease |
ID |
| Diagnosis/Initial |
intellectual disability |
| Diagnosis/Definite |
WITKOS |
| Inheritance |
Familial, autosomal dominant |
| Phenotype details |
see paper; ..., intellectual disability (TIQ <70); OFC percentile <P3; height percentile <P3; no autism spectrum disorder; no epilepsy; delayed bone age; no hearing loss; typical facial dysmorphic features |
| Age/Examination |
16y3m (16 years, 3 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-10-09 15:12:14 +02:00 (CEST) |
| Date last edited |
N/A |