Phenotype #0000010379
| Individual ID |
00011692 |
| Associated disease |
GA1 |
| Inheritance |
Familial, autosomal recessive |
| Age/Onset |
00y11m |
| Diagnosis/Initial |
- |
| Age/Examination |
01y00m (1 year) |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
- |
| Phenotype/Onset |
- |
| Phenotype details |
regression, dystonia, seizure, athetosis, macrocephaly, MRI: basal nuclei malacia |
| Protein |
- |
| Biochem |
3-OH-GA(urine): 58.56 (fold change vs. normal control); GA(urine): 359.07 (fold change vs. normal control) |
| Enzyme/Activity |
- |
| Owner name |
Svenja Wagner |
| Database submission license |
No license selected |
| Created by |
Svenja Wagner |
| Date created |
2014-02-20 13:48:05 +01:00 (CET) |
| Date last edited |
2014-04-28 13:36:26 +02:00 (CEST) |
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