Phenotype #0000223172
| Individual ID |
00295607 |
| Associated disease |
HHF3 |
| Phenotype details |
ORPHA:79299 HP:0005978 HP:0008283 HP:0001988 HP:0001985 HP:0000825 |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal dominant |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Fanny Kortüm |
| Database submission license |
No license selected |
| Created by |
Fanny Kortüm |
| Date created |
2020-03-18 11:30:51 +01:00 (CET) |
| Date last edited |
2020-03-19 15:13:39 +01:00 (CET) |
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