neutropenia, severe congenital, 2, autosomal dominant
MONDO:0013139Also 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
- MONDO:
- MONDO:0013139
- OMIM:
- 613107 ↗
Rare disease33 associated genes
Description
Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.
Associated genes
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