Phenotype #0000186925
| Individual ID |
00247693 |
| Associated disease |
F13BD |
| Phenotype details |
complete deficiency of FXIII B subunit |
| Diagnosis/Initial |
- |
| Inheritance |
- |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Carville G. Bevans |
| Database submission license |
No license selected |
| Created by |
Carville G. Bevans |
| Date created |
2013-06-12 18:16:32 +02:00 (CEST) |
| Date last edited |
2013-06-14 11:08:33 +02:00 (CEST) |
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