Phenotype #0000141830
| Individual ID |
00177013 |
| Associated disease |
EE |
| Phenotype details |
HP:0001252 HP:0002066 HP:0100807 HP:0006184 HP:0000767 |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
Epileptic encephalopathy, early infantile, 13 |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
00y03m |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Anaïs Begemann |
| Database submission license |
No license selected |
| Created by |
Anaïs Begemann |
| Date created |
2018-08-16 11:44:17 +02:00 (CEST) |
| Date last edited |
2018-08-17 11:38:37 +02:00 (CEST) |
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