Tyrosinemia type 1, FAH-related, rabbit

MONDO:1010721

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.

Also known as: tyrosinemia type I, rabbit

0 clinical trials for this condition and its sub-types, 0 tagged with Tyrosinemia type 1, FAH-related, rabbit itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary disease, non-human animal (9) ↑ Metabolic disease, non-human animal (9)

Including sub-types (0) Tagged with Tyrosinemia type 1, FAH-related, rabbit (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.