Disease #01636 (SCN1 (neutropenia, congenital, severe, autosomal dominant (SCN1)), OMIM:202700)

Official abbreviation SCN1
Name neutropenia, congenital, severe, autosomal dominant (SCN1)
OMIM ID 202700
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ELANE
Associated tissues -
Disease features -
Remarks -