Disease association ontology term - MONDO:0014118 - congenital neutropenia-myelofibrosis-nephromegaly syndrome
Term summary
ID
MONDO:0014118
Name
congenital neutropenia-myelofibrosis-nephromegaly syndrome
Ontology or CV name
Disease association
Parents
is_a
autosomal recessive severe congenital neutropenia
Annotation
Disease association
MONDO:0014118
-
congenital neutropenia-myelofibrosis-nephromegaly syndrome
References:
PB_REF:0000003
PB_REF:0000006
Genes:
pep7 (SPAC17G6.08)
vps45 (SPAC2G11.03c)