Phenotype #0000026565
Individual ID |
00033136 |
Associated disease |
- |
Phenotype details |
congenital stationary night blindness |
Diagnosis/Initial |
retinitis pigmentosa |
Inheritance |
Unknown |
Diagnosis/Definite |
- |
Age/Examination |
0d |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Kornelia Neveling |
Database submission license |
No license selected |
Created by |
Kornelia Neveling |
Date created |
2012-02-04 14:49:23 +01:00 (CET) |
Date last edited |
2020-08-25 10:48:31 +02:00 (CEST) |
|