Phenotype #0000144218
Individual ID |
00183513 |
Associated disease |
OPMD |
Phenotype details |
more sever phenotype |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
OPMD |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2011-01-16 11:38:09 +01:00 (CET) |
Date last edited |
2012-03-09 20:07:18 +01:00 (CET) |
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