| Dataset | HuGE Navigator Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An abnormal reduction in the amount of pigmentation (reduced or absent) of skin, hair and eye (iris and retina). (Human Phenotype Ontology, HP_0001022) |
| Similar Terms | |
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2 genes associated with the Albinism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
