Tyrosinemia type 1

Tyrosinemia type I is a genetic disorder that disrupts the metabolism of the amino acid tyrosine, resulting in damage primarily to the liver along with the kidneys and peripheral nerves. The inability of cells to process tyrosine can lead to chronic liver damage ending in liver failure, as well as renal disease and rickets. [Source: Wikipedia ]

Synonyms
Hepatorenal tyrosinemia
Type 1 tyrosinemia
OrphaNet reference
Tyrosinemia type 1 
Is A
Tyrosinemia
May Cause
Anemia
Ascites
Cirrhosis
Congenital hepatomegaly
Congenital splenomegaly