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Severe Congenital Neutropenia — Gene Therapy & Clinical Trials | FollowGene
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Severe Congenital Neutropenia
Severe Congenital Neutropenia
Prevalence:
1/200000
hematologic
Official
·
OMIM:202700
Official
·
ORPHA486
Severe neutrophil deficiency due to ELANE or HAX1 gene mutations.
Associated Genes
ELANE
Elastase Neutrophil Expressed
Chromosome 19
Autosomal Dominant
HAX1
HCLS1 Associated Protein X-1
Chromosome 1
Autosomal Recessive