autosomal recessive severe congenital neutropenia due to CXCR2 deficiency

Findings

No curated finding names autosomal recessive severe congenital neutropenia due to CXCR2 deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• autosomal recessive severe congenital neutropenia