Phenotype #0000309963
| Individual ID |
00418627 |
| Associated disease |
NDD |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., birth 38w, pregnancy/delivery uncomplicated; weight 15th%, Height 24th%, OFC 3rd-10th%; motor delay; speech delay; high nasal bridge, upturned nasal tip, mildly down-slanting palpebral fissures, high-arched palate with dental crowding, retrognathia, long-appearing fingers, dysplastic toenails, pronated feet; poor feeding; hypotonia; velopharyngeal insufficiency; astigmatism; male cousin with possible pervasive developmental delay |
| Inheritance |
Unknown |
| Age/Examination |
03y09m (3 years, 9 months) |
| 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 |
2022-10-03 11:24:02 +02:00 (CEST) |
| Date last edited |
N/A |
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