|
MIM:618752 - NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT; SCN8
Xenbase Genes:
Human Disease Resource: OMIM
MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant |
DOID:0112135 - severe congenital neutropenia 8 |
|
MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant |
DOID:0112135 - severe congenital neutropenia 8 |