Phenotype #0000171761
| Individual ID |
00226649 |
| Associated disease |
THMD |
| Diagnosis/Initial |
biotin responsive basal ganglia disease |
| Diagnosis/Definite |
THMD-2 |
| Phenotype details |
neuroimaging abnormalities: caudate, putamen, globus pallidus, lactate on MRS; outcome: spasticity, seizures, hypotonia, intellectual disability, dystonia |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
12y (12 years) |
| Age/Diagnosis |
- |
| Age/Onset |
21m |
| 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 |
2019-03-09 21:20:59 +01:00 (CET) |
| Date last edited |
N/A |
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