Phenotype #0000331120
| Individual ID |
00441695 |
| Associated disease |
NDD |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., microcephaly; global developmental delay; 3y-walk; language severely delayed; severe intellectual disability; no seizures; peripheral neuropathy; ataxia; no dysmorphic features; tone reduced; power reduced; sensation reduced; ataxic gait; |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
21y (21 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-11-09 12:18:41 +01:00 (CET) |
| Date last edited |
N/A |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|