Disease association ontology term - MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant

Term summary

ID: MONDO:0032899
Name: neutropenia, severe congenital, 8, autosomal dominant
Ontology or CV name: Disease association

Parents

is_a severe congenital neutropenia

Annotation

Disease association

MONDO:0032899 - neutropenia, severe congenital, 8, autosomal dominant

References:

PB_REF:0000006

Genes:

srp54 (SPCC188.06c)