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) |
|