OBO ID: DOID:0112130 |
Term Name: | autosomal dominant severe congenital neutropenia | Search Ontology: | |
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Definition: | A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene. (2) | ||
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Ontology: | Human Disease ( DOID:0112130 ) |
OTHER autosomal dominant severe congenital neutropenia PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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