Phenotype #0000084462
| Individual ID |
00106656 |
| Associated disease |
ID |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Inheritance |
Isolated (sporadic) |
| Phenotype details |
HP:0001249; HP:0100851; HP:0000478; HP:0000256; HP:0025031; HP:0001629; intellectual disability (HP:0001249); no speech delay (-HP:0000750) |
| Age/Examination |
03y09m (3 years, 9 months) |
| 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 11:38:21 +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.
|