Phenotype #0000000925
Individual ID |
00001771 |
Associated disease |
EDS |
Inheritance |
Unknown |
Diagnosis/Initial |
- |
Age/Examination |
- |
Diagnosis/Definite |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Phenotype details |
ascertainment ; clinical presentation |
Hearing/Loss |
- |
Protein |
- |
CK-level |
- |
EMG |
- |
Muscle/Biopsy |
- |
Age/Diagnosis |
- |
Owner name |
Division of Human Genetics, Innsbruck |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Division of Human Genetics, Innsbruck |
Date created |
2010-07-29 15:29:14 +02:00 (CEST) |
Date last edited |
N/A |
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