Phenotype #0000044619
Individual ID |
00057988 |
Associated disease |
TMD |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Initial |
- |
Age/Examination |
- |
Diagnosis/Definite |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Phenotype details |
- |
Protein |
- |
Owner name |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2012-02-26 15:41:30 +01:00 (CET) |
Date last edited |
2015-11-08 09:35:54 +01:00 (CET) |
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