Search Ontology:
Human Disease

autosomal dominant severe congenital neutropenia

Term ID
DOID:0112130
Synonyms
Definition
A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene. (2)
References
  • GARD:9558
  • ORDO:486
Ontology
Human Disease   ( DOID:0112130 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models