Phenotype #0000015239
| Individual ID |
00016698 |
| Associated disease |
HOMG1 |
| Phenotype details |
initial Mg2+ 0.21 mM, FE Mg2+ 4.8%; age onset 9w |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
seizures |
| Protein |
- |
| Owner name |
Karl Schlingmann |
| Database submission license |
No license selected |
| Created by |
Johan den Dunnen |
| Date created |
2014-05-30 14:11:42 +02:00 (CEST) |
| Date last edited |
N/A |
|