Individual ID |
00207521 |
Associated disease |
BVVLS1 |
Phenotype details |
Visual impairment (HP:0000505) Hearing impairment (HP:0000365) |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
BVVLS |
Age/Examination |
- |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Gunnar Schmidt |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Gunnar Schmidt |
Date created |
2018-11-23 18:16:47 +01:00 (CET) |
Date last edited |
2018-11-23 19:28:06 +01:00 (CET) |