WormBase Tree Display for DO_term: DOID:0050725
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| DOID:0050725 | Name | tyrosinemia type II | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A tyrosinemia that has_material_basis_in deficiency of hepatic tyrosine aminotransferase located_in the liver and is characterized by keratitis, painful palmoplantar hyperkeratosis, mental retardation, and elevated serum tyrosine levels. | ||||
| Synonym | Exact | Oculocutaneous tyrosinemia | |||
| Richner-Hanhart syndrome | |||||
| Parent | Is_a | DOID:37 | |||
| DOID:409 | |||||
| DOID:9275 | |||||
| DB_info | Database | OMIM | disease | 276600 | |
| Attribute_of | Gene_by_orthology | WBGene00009628 |
