| Individual ID |
00424829 |
| Associated disease |
DD |
| Phenotype details |
Intrauterine growth retardation (HP:0001511); Caesarian section (HP:0011410); Premature birth (HP:0001622); Respiratory failure requiring assisted ventilation (HP:0004887); Motor delay (HP:0001270); Speech delay (HP:0000750); Intellectual disability (HP:0001249); Intellectual disability, mild (HP:0001256); Preauricular skin tag (HP:0000384); Hypertelorism (HP:0000316); Broad toe (HP:0001837); Long fingers (HP:0100807); Low-set ears (HP:0000369); Retrognathia (HP:0000278) |
| Diagnosis/Initial |
- |
| Inheritance |
Unknown |
| Diagnosis/Definite |
- |
| Age/Examination |
19y (19 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Frederike Leonie Harms |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Frederike Leonie Harms |
| Date created |
2022-11-22 15:08:32 +01:00 (CET) |
| Date last edited |
2022-12-19 16:47:44 +01:00 (CET) |