Phenotype #0000207626
| Individual ID |
00269835 |
| Associated disease |
ID |
| Diagnosis/Initial |
intellectual disability |
| Diagnosis/Definite |
- |
| Inheritance |
Familial, autosomal recessive |
| Phenotype details |
see paper; ..., 6y-deceased; signs of cerebral palsy, no speech, nonambulant; generalized tonic clonic seizures; severe brain atrophy |
| Age/Examination |
06y (6 years) |
| 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 |
2019-12-07 13:20:49 +01:00 (CET) |
| Date last edited |
2019-12-07 14:30:32 +01:00 (CET) |
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