Neutropenia, severe congenital, 2, autosomal dominant

MONDO:0013139

Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.

Also known as: GFI1 autosomal dominant severe congenital neutropenia, autosomal dominant severe congenital neutropenia caused by mutation in GFI1, neutropenia, severe congenital 2, autosomal dominant, neutropenia, severe congenital, 2, autosomal dominant, SCN2

0 clinical trials for this condition and its sub-types, 0 tagged with Neutropenia, severe congenital, 2, autosomal dominant itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Autosomal dominant severe congenital neutropenia (0)

Including sub-types (0) Tagged with Neutropenia, severe congenital, 2, autosomal dominant (0)

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