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neutropenia, severe congenital, 2, autosomal dominant

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any autosomal dominant severe congenital neutropenia in which the cause of the disease is a mutation in the GFI1 gene.
Uniprot Description A disorder of hematopoiesis characterized by maturation arrest of granulopoiesis at the level of promyelocytes with peripheral blood absolute neutrophil counts below 0.5 x 10(9)/l and early onset of severe bacterial infections.
Mondo Term and Equivalent IDs
MONDO:0013139:  neutropenia, severe congenital, 2, autosomal dominant
MESH:C567748: 
UMLS:C2751288: