Phenotype #0000087483
| Individual ID |
00111398 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
mild intellectual disability (HP:0001256); mild global developmental delay (HP:0011342); no speech delay (-HP:0000750) |
| 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 01:03:56 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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