Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency

Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency (disorder)

active
Code783200000
Semantic tagdisorder
Moduleinternational
Definitionprimitive
Effective time20190731

Synonyms

Parents (2)

Children (0)

None (leaf concept).