Phenotype #0000128919
| Individual ID |
00163799 |
| Associated disease |
CPDX2 |
| Phenotype details |
severe fetal form |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, X-linked |
| Diagnosis/Definite |
CPDX-2 |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Fabienne Dufernez |
| Database submission license |
No license selected |
| Created by |
Fabienne Dufernez |
| Date created |
2018-04-12 16:40:28 +02:00 (CEST) |
| Date last edited |
2018-04-12 16:48:06 +02:00 (CEST) |
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