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X-linked severe congenital neutropenia

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description This syndrome is an immunodeficiency syndrome characterized by recurrent major bacterial infections, severe congenital neutropenia, and monocytopenia. It has been described in five males spanning three generations of one family. It is transmitted as an X-linked recessive trait and is caused by mutations in the WAS gene, encoding the WASP protein.
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:0010294:  X-linked severe congenital neutropenia
GARD:0003981: 
MESH:C564539: 
Orphanet:86788: 
SCTID:718882006: 
UMLS:C1845987: