Test Background

Mutations in HAX1 result in severe congenital neutropenia/Kostmann disease, which are disorders of hematopoiesis. There are several types. This particular type is inherited in an autosomal recessive manner.

This laboratory performs Sanger sequencing of the HAX1 gene.

Gene(s)

HAX1

Vital Information

Test Code:
S0864

Turnaround Time:
3-5 weeks

CPT Code:
81479×1

Billing

Forms and Documents