Disease association ontology term - MONDO:0030726 - neutropenia, severe congenital, 9, autosomal dominant

Term summary

ID: MONDO:0030726
Name: neutropenia, severe congenital, 9, autosomal dominant
Ontology or CV name: Disease association

Parents

is_a severe congenital neutropenia

Annotation

Disease association

MONDO:0030726 - neutropenia, severe congenital, 9, autosomal dominant

References:

PB_REF:0000003

Genes:

aqp1 (SPAC977.17)