Phenotype #0000087493
| Individual ID |
00111408 |
| Associated disease |
BRNRS |
| Phenotype details |
Male, 7 y, speech delay, moderate ID, behavioral anomalies (maternal XI 82%) |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, X-linked recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Bernt Popp |
| Database submission license |
No license selected |
| Created by |
Bernt Popp |
| Date created |
2017-08-03 07:32:27 +02:00 (CEST) |
| Date last edited |
2017-08-04 09:29:30 +02:00 (CEST) |
|