Phenotype #0000124291
| Individual ID |
00151928 |
| Associated disease |
WHS |
| Phenotype details |
7m-onset seizures; status epilepticus; severe developmental delay, 1y5m-roll over; height/weight (SD) -6.4/-3.7; tube feeding; no cleft lip/cleft palate; no heart defect; no urogenital defect; no skeletal abnormality; nasolacrimal duct obstruction; moderate hearing impairment; Fanconi syndrome due to valproate |
| Diagnosis/Initial |
Wolf-Hirschhorn syndrome |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
WHS |
| Age/Examination |
6y6m (6 years, 6 months) |
| 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 |
2018-01-28 09:38:22 +01:00 (CET) |
| Date last edited |
2018-01-28 10:21:36 +01:00 (CET) |
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