Phenotype #0000084332
| Individual ID |
00106519 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
mild Developmental delay/Intellectual disability, mild speech/language delay, Motor delay, Large helices of both ears (similar to father),; mild intellectual disability (HP:0001256); mild global developmental delay (HP:0011342); mild speech delay (HP:0000750) |
| Age/Examination |
10y09m (10 years, 9 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Bernt Popp |
| Database submission license |
No license selected |
| Created by |
Bernt Popp |
| Date created |
2017-07-02 21:25:57 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
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