Phenotype #0000236429
| Individual ID |
00311176 |
| Associated disease |
BBSOAS |
| Phenotype details |
Caesarian section (HP:0011410); Cupped ear (HP:0000378); Narrow mouth (HP:0000160); Sloping forehead (HP:0000340); Delayed ability to walk (HP:0031936); Delayed speech and language development (HP:0000750); Astigmatism (HP:0000483); Autistic behavior (HP:0000729); Aggressive behavior (HP:0000718); Generalized-onset seizure (HP:0002197); EEG with central focal spikes (HP:0012014) |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
21y (21 years) |
| Age/Diagnosis |
- |
| Age/Onset |
? |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Benjamin Billiet |
| Database submission license |
No license selected |
| Created by |
Benjamin Billiet |
| Date created |
2020-09-21 11:11:13 +02:00 (CEST) |
| Date last edited |
2021-05-05 16:34:12 +02:00 (CEST) |
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