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
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