neutropenia, severe congenital, 2, autosomal dominant

Rare Disease

MONDO:0013139

Also known as:

GFI1 autosomal dominant severe congenital neutropeniaautosomal dominant severe congenital neutropenia caused by mutation in GFI1neutropenia, severe congenital 2, autosomal dominant

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

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Companies Active in neutropenia, severe congenital, 2, autosomal dominant

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Amgen Inc

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neutropenia, severe congenital, 2, autosomal dominant

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Companies Active in neutropenia, severe congenital, 2, autosomal dominant