Disease #02146 (SCNX (neutropenia, congenital, severe, X-linked (SCNX)), OMIM:300299)

Official abbreviation SCNX
Name neutropenia, congenital, severe, X-linked (SCNX)
OMIM ID 300299
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WAS
Associated tissues -
Disease features -
Remarks -