| Individual ID |
00324491 |
| Associated disease |
? |
| Diagnosis/Initial |
- |
| Diagnosis/Definite |
- |
| Phenotype details |
no prenatal growth retardation (−2SDs); postnatal growth retardation (−2SDs); no developmental delay/intellectual disability; no speech delay; no hypotonia; no microcephaly (−2SDs); long/triangular face; high forehead; high nasal bridge; long nose; no thick lips; short chin; pointed china; no Pierre Robin sequence/cleft palate; dental crowding; skeletal anomalies; short hands/brachydactyly; no hip defects; no thin/short long bones; no squared vertebrae; no abnormal cervical vertebrae; no 11 pairs of ribs; no scoliosis; limited flexions fingers, hand grip difficulties; no hearing loss (conductive); no cardiac defects |
| Inheritance |
Familial, autosomal recessive |
| Age/Examination |
8y (8 years) |
| 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 |
2020-12-14 19:34:41 +01:00 (CET) |
| Date last edited |
N/A |