Phenotype #0000080269
Individual ID |
00102083 |
Associated disease |
ID |
Diagnosis/Initial |
- |
Diagnosis/Definite |
- |
Inheritance |
Isolated (sporadic) |
Phenotype details |
HP:0001999; HP:0001182; HP:0006101; HP:0002650; intellectual disability (HP:0001249) |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Wenjuan Qiu |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Wenjuan Qiu |
Date created |
2017-03-30 08:51:34 +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.
|