Phenotype #0000347520
| Individual ID |
00459446 |
| Associated disease |
NDD |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., intrauterine growth restriction, developmental delay; secondary microcephaly; moderate intellectual disability; delayed speech; delayed motor development, not walking; no spasticity; no ataxia; no seizures; apraxia, horizontal gaze palsy; hearing impairment; joint laxity; facial dysmorphism; high arched palate; 4m-neuroimaging thin corpus callosum (detailed in paper) |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
17m |
| Age/Diagnosis |
- |
| Age/Onset |
0d |
| 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 |
2025-01-04 12:10:18 +01:00 (CET) |
| Date last edited |
N/A |
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