Phenotype #0000010362
| Individual ID |
00011673 |
| Associated disease |
GA1 |
| Inheritance |
Familial, autosomal recessive |
| Age/Onset |
00y04m |
| Diagnosis/Initial |
- |
| Age/Examination |
00y10m (10 months) |
| Diagnosis/Definite |
- |
| Age/Diagnosis |
- |
| Phenotype/Onset |
- |
| Phenotype details |
retardation, dystonia, macrocephaly |
| Protein |
- |
| Biochem |
glutarylcarnitine(blood): 0.50 µM/L (c: 0.02-0.20); 3-OH-GA(urine): 14.47 (fold change vs. normal control); GA(urine): 3557.39 (fold change vs. normal control) |
| Enzyme/Activity |
- |
| Owner name |
Svenja Wagner |
| Database submission license |
No license selected |
| Created by |
Svenja Wagner |
| Date created |
2014-02-18 13:15:55 +01:00 (CET) |
| Date last edited |
2014-04-03 14:29:41 +02:00 (CEST) |
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