Disease #05207 (OCA1 (albinism, oculocutaneous, type I (OCA-1)))
Official abbreviation |
OCA1 |
Name |
albinism, oculocutaneous, type I (OCA-1) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
212 |
Phenotype entries for this disease |
212 |
Associated with 1 gene |
TYR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2016-12-02 17:47:10 +01:00 (CET) |
Date last edited |
2021-12-11 13:56:28 +01:00 (CET) |
Individuals
|