| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | An amino acid metabolic disorder that involves phenylalanine and tyrosine metabolism with the accumulation of homogentisic acid, a toxic tyrosine byproduct. (Human Disease Ontology, DOID_9270) |
| Similar Terms | |
| Downloads & Tools |
1 genes involed in the disease alkaptonuria from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
| Symbol | Name |
|---|---|
| HGD | homogentisate 1,2-dioxygenase |
