A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH), which is needed to break down the amino acid tyrosine.
More information
More information
Related categories 2
Sites 2
Offers the synonyms, a general discussion and further resources.
Factsheet on this disorder of tyrosine metabolism, its description, epidemiology, presentation, differential diagnosis, investigations, associated diseases, management, complications, prognosis and prevention.
Factsheet on this disorder of tyrosine metabolism, its description, epidemiology, presentation, differential diagnosis, investigations, associated diseases, management, complications, prognosis and prevention.
Offers the synonyms, a general discussion and further resources.
Last update:
September 25, 2015 at 18:04:22 UTC
Check out
Regional: Europe: United Kingdom: England: London: Hackney: Business and Economy: Event Planning: Caterers
- Recently edited by merlin1
- Recently edited by merlin1