Search Ontology:
Human Disease

severe congenital neutropenia 1

Term ID
DOID:0080625
Synonyms
Definition
A severe congenital neutropenia that has_material_basis_in heterozygous mutation in the neutrophil elastase gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/17133096
References
Ontology
Human Disease   ( DOID:0080625 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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