Phenotype #0000351161
| Individual ID |
00465618 |
| Associated disease |
ID |
| Diagnosis/Initial |
intellectual disability |
| Diagnosis/Definite |
MRXSHG |
| Inheritance |
Familial, X-linked recessive |
| Phenotype details |
see paper; ..., developmental delay; speech delay; mild-moderate intellectual disability; epilepsy/seizures; borderline microcephaly; attention deficit hyperactivity disorder |
| Age/Examination |
05y (5 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-05-27 19:53:16 +02:00 (CEST) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|