| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine. (Human Disease Ontology, DOID_0050727) |
| External Link | http://www.omim.org/entry/276710 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the tyrosinemia, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| HPD | 4-hydroxyphenylpyruvate dioxygenase |
