| Metadata | |
|---|---|
| ID | DOID:0112133 |
| Name | severe congenital neutropenia 3 |
| Definition | A severe congenital neutropenia characterized by bone marrow failure resulting in low numbers of neutrophils, increased susceptibility to bacterial and fungal infections, and increased risk of developing myelodysplastic syndrome or acute myeloid leukemia that has_material_basis_in homozygous or compound heterozygous mutation in the HAX1 gene on chromosome 1q21.3. https://pubmed.ncbi.nlm.nih.gov/21108402/, https://pubmed.ncbi.nlm.nih.gov/17187068/ |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
infantile agranulocytosis [EXACT] Kostmann disease [EXACT] Kostmann syndrome [EXACT] SCN3 [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance disease has basis in some Abnormality of prenatal development or birth |