severe congenital neutropenia 3

Summary
Synonym
  • Kostmann disease
  • Kostmann syndrome
  • SCN3
  • infantile agranulocytosis
Definition
A severe congenital neutropenia characterized by bone marrow failure resulting in low numbers of neutrophils, increased susceptibility to bacterial and fungal infections, and increased risk of developing myelodysplastic syndrome or acute myeloid leukemia that has_material_basis_in homozygous or compound heterozygous mutation in the HAX1 gene on chromosome 1q21.3.
Super Class
autosomal recessive disease severe congenital neutropenia
Disease Ontology
DOID:0112133
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10456 HAX1 HCLS1 associated protein X-1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024