All diseases

OMIM ID
276700
OMIM term:
TYROSINEMIA, TYPE I
Alternative terms:
HEPATORENAL TYROSINEMIA
FUMARYLACETOACETASE DEFICIENCY
FAH DEFICIENCY
(∗) Location:
15q25.1  
(†) Associated OMIM genes:
FAH  
(‡) Associated MGI genes:
Fah  

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