FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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Term severe congenital neutropenia 1 ID (Ontology) DOID:0080625 (Human Disease)
Definition A severe congenital neutropenia that has_material_basis_in heterozygous mutation in the neutrophil elastase gene on chromosome 19p13.
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 Genes
 severe congenital neutropenia 1       9
 for disease ribbon | severe congenital neutropenia 1       9
 model of | severe congenital neutropenia 1       9
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease_____
physical disorder                  |
 |__severe congenital neutropenia__|
neutropenia                        |
 |__severe congenital neutropenia__|
                                   severe congenital neutropenia 1  9 rec.
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Is a severe congenital neutropenia
autosomal dominant disease
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MIM:202700