All diseases

OMIM ID
276710
OMIM term:
TYROSINEMIA, TYPE III
Alternative terms:
4-@HYDROXYPHENYLPYRUVIC ACID OXIDASE DEFICIENCY
4-@HYDROXYPHENYLPYRUVATE DIOXYGENASE DEFICIENCY
(∗) Location:
12q24.31  
(†) Associated OMIM genes:
HPD  
(‡) Associated MGI genes:
Hpd  

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* quick link - http://q.sanger.ac.uk/nqb173j5