Phenotype #0000186536
Individual ID |
00246692 |
Associated disease |
SPG |
Phenotype details |
- |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal dominant |
Diagnosis/Definite |
- |
Age/Examination |
03y (3 years) |
Age/Diagnosis |
03y |
Age/Onset |
01y |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Maartje Pennings |
Database submission license |
No license selected |
Created by |
Maartje Pennings |
Date created |
2019-07-16 13:27:54 +02:00 (CEST) |
Date last edited |
2019-07-16 17:45:29 +02:00 (CEST) |
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