Fanconi anemia complementation group I

MONDO:0012186

Fanconi anemia caused by mutations in the FANCI gene, encoding Fanconi anemia group I protein.

Also known as: FANCI, Fanconi Anemia, complementation group type 1, Fanconi anaemia complementation group type I, Fanconi anemia complementation group I, Fanconi anemia complementation group type I, Fanconi Anemia, complementation Group 1, Fanconi anemia, complementation group I

12 clinical trials for this condition and its sub-types, 0 tagged with Fanconi anemia complementation group I itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Fanconi anemia (42)

Including sub-types (12) Tagged with Fanconi anemia complementation group I (0)

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