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severe congenital neutropenia 1
Summary
- Definition
- A severe congenital neutropenia that has_material_basis_in heterozygous mutation in the neutrophil elastase gene on chromosome 19p13.
- Super Class
- autosomal dominant disease severe congenital neutropenia
External Links
- Disease Ontology
- DOID:0080625
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002718 | Recurrent bacterial infections |
| HP:0001880 | Eosinophilia |
| HP:0006721 | Acute lymphoblastic leukemia |
| HP:0000938 | Osteopenia |
| HP:0004798 | Recurrent infection of the gastrointestinal tract |
| HP:0100658 | Cellulitis |
| HP:0001945 | Fever |
| HP:0000230 | Gingivitis |
| HP:0002027 | Abdominal pain |
| HP:0005425 | Recurrent sinopulmonary infections |
