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Up to: Hereditary disease, non-human animal · Metabolic disease, non-human animal
Tyrosinemia type 1, FAH-related, rabbit
Any deficiency in fumarylacetoacetate hydrolase that occurs in rabbits due to a mutation in the FAH gene created by genetic engineering or gene editing. Fumarylacetoacetate hydrolase is an enzyme that catalyzes the last step of tyrosine metabolism.
This condition has no sub-types.