Phenotype #0000239717
| Individual ID |
00315972 |
| Associated disease |
? |
| Diagnosis/Initial |
neurodevelopmental delay |
| Diagnosis/Definite |
- |
| Phenotype details |
see paper; ..., failure to thrive; no globe defect; no coloboma; visual impairment; Intermittent exotropia; no motor delay; speech delay; aggression, biting, phonosensitivity, pacing; hypotonia; no cardiac defect; no kidney anomaly; left eye diaphragmatic hernia; thin upper lip |
| Inheritance |
Isolated (sporadic) |
| Age/Examination |
03y08m (3 years, 8 months) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Tumor/MSI |
- |
| Diagnosis/Criteria |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-11-01 10:06:29 +01:00 (CET) |
| Date last edited |
2022-11-30 19:27:50 +01:00 (CET) |
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