Phenotype #0000325298
| Individual ID |
00435061 |
| Associated disease |
NDD |
| Diagnosis/Initial |
NDD |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., 13y-deceased; global developmental delay; intellectual disability; language delay; impaired motor development; MRI brain mildly dilated 4th ventricle, suspected mild atrophy cerebellum; hypotonia; no seizures; microcephaly; no optic findings; prenatal microcephaly; coarse facial features, broad nose, large mouth |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
13y (13 years) |
| 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 |
2023-05-05 15:10:52 +02:00 (CEST) |
| Date last edited |
N/A |
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