Phenotype #0000331118
| Individual ID |
00441693 |
| Associated disease |
NDD |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., microcephaly; global developmental delay; 2y-sit; 3y-walk; language severely delayed; moderate intellectual disability; generalised tonic clonic seizures; |
| 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 |
2023-11-09 12:18:41 +01:00 (CET) |
| Date last edited |
N/A |
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