- OMIM ID
-
276600
- OMIM term:
- TYROSINEMIA, TYPE II
- Alternative terms:
-
RICHNER-HANHART SYNDROME
TYROSINE AMINOTRANSFERASE DEFICIENCY
TAT DEFICIENCY
TYROSINE TRANSAMINASE DEFICIENCY
KERATOSIS PALMOPLANTARIS WITH CORNEAL DYSTROPHY
OREGON TYPE TYROSINEMIA
TYROSINOSIS, OCULOCUTANEOUS TYPE
- (∗) Location:
- 16q22.2
- (†) Associated OMIM genes:
- TAT
- (‡) Associated MGI genes:
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