Phenotype #0000084408
| Individual ID |
00106601 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
HP:0001263; HP:0001249; HP:0000750; HP:0002194; HP:0100851; intellectual disability (HP:0001249); global developmental delay (HP:0001263); speech delay (HP:0000750) |
| Age/Examination |
04y (4 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Sébastien Küry |
| Database submission license |
No license selected |
| Created by |
Sébastien Küry |
| Date created |
2017-07-07 10:33:56 +02:00 (CEST) |
| Date last edited |
2020-05-12 12:33:06 +02:00 (CEST) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|