Phenotype #0000206955
Individual ID |
00267238 |
Associated disease |
MRT |
Phenotype details |
- |
Diagnosis/Initial |
intellectual disability |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
MRT42 |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Isabel Filges |
Database submission license |
No license selected |
Created by |
Johan den Dunnen |
Date created |
2019-11-05 22:50:15 +01:00 (CET) |
Date last edited |
N/A |
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