Tyrosinemia Type II
| Disease Aliases (19) | Deficiency of tyrosine aminotransferase Hereditary hypertyrosinemia, type ii Hypertyrosinemia, oregon type Hypertyrosinemia, richner-hanhart type Keratosis palmoplantaris with corneal dystrophy Keratosis palmoplantaris-corneal dystrophy syndrome Oculocutaneous tyrosinemia Oregon type tyrosinemia Persistent hypertyrosinemia Richner syndrome Richner-hanhart syndrome Tat deficiency Tat-gene related hypertyrosinemia richner hanhart type Tyrosine aminotransferase deficiency Tyrosine transaminase deficiency Tyrosinemia due to tat deficiency Tyrosinemia due to tyrosine aminotransferase deficiency Tyrosinemia type 2 Tyrosinemia without hepatorenal dysfunction |
Associated Genes (0) | |||||||
| Cross-references of Tyrosinemia type II | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |