Phenotype #0000087485
| Individual ID |
00111400 |
| Associated disease |
PTHS |
| Phenotype details |
Hypotonia, developmental delay |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Bernt Popp |
| Database submission license |
No license selected |
| Created by |
Bernt Popp |
| Date created |
2017-08-03 01:10:53 +02:00 (CEST) |
| Date last edited |
2017-08-04 09:29:30 +02:00 (CEST) |
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