Phenotype #0000020227
| Individual ID |
00024129 |
| Associated disease |
MRT |
| Phenotype details |
Severe, non-specific, autosomal recessive intellectual disability |
| Diagnosis/Initial |
- |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
- |
| Age/Examination |
05y (5 years) |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Rami Abou Jamra |
| Database submission license |
No license selected |
| Created by |
Rami Abou Jamra |
| Date created |
2014-10-29 13:07:08 +01:00 (CET) |
| Date last edited |
2014-10-31 15:05:37 +01:00 (CET) |
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