| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/203200 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the {albinism, oculocutaneous, type ii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| MC1R | melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) |
