All diseases

OMIM ID
610738
OMIM term:
NEUTROPENIA, SEVERE CONGENITAL, 3, AUTOSOMAL RECESSIVE; SCN3
Alternative terms:
KOSTMANN DISEASE
AGRANULOCYTOSIS, INFANTILE
(∗) Location:
1q21.3  
(†) Associated OMIM genes:
HAX1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/9mxl2078