Phenotype #0000015243
| Individual ID |
00016708 |
| Associated disease |
HOMG1 |
| Phenotype details |
initial Mg2+ 0.17 mM, FE Mg2+ 4.5%; age onset 5w |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
00y01m |
| Phenotype/Onset |
seizures |
| Protein |
- |
| Owner name |
Karl Schlingmann |
| Database submission license |
No license selected |
| Created by |
Johan den Dunnen |
| Date created |
2014-05-30 14:31:30 +02:00 (CEST) |
| Date last edited |
N/A |
|