Phenotype #0000232680
| Individual ID |
00306852 |
| Associated disease |
Gilbert syndrome |
| Phenotype details |
Kernicterus, anemia, unconjugated hyperbilirubinemia |
| Diagnosis/Initial |
- |
| Inheritance |
Familial |
| Diagnosis/Definite |
- |
| Age/Examination |
17y (17 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Nawel Trabelsi |
| Database submission license |
No license selected |
| Created by |
Nawel Trabelsi |
| Date created |
2020-07-21 16:39:04 +02:00 (CEST) |
| Date last edited |
2020-09-11 11:47:26 +02:00 (CEST) |
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