Disease #04532 (SCN6 (neutropenia, severe congenital, type 6, autosomal recessive (SCN-6)), OMIM:616022)

Official abbreviation SCN6
Name neutropenia, severe congenital, type 6, autosomal recessive (SCN-6)
OMIM ID 616022
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene JAGN1
Associated tissues -
Disease features -
Remarks -