Phenotype #0000020186
Individual ID |
00022415 |
Associated disease |
MRT |
Phenotype details |
mild intellectual disability and epilepsy; no signs of myopathy |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
- |
Age/Examination |
>26y (later than 26 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Arnaud Vanlander |
Database submission license |
No license selected |
Created by |
Johan den Dunnen |
Date created |
2014-10-11 12:23:37 +02:00 (CEST) |
Date last edited |
N/A |
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