{
    "disease_id": "DOID:0090120",
    "recommended_name": {
        "id": "DOID:0090120",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0090120",
        "name": "hereditary neutrophilia",
        "description": "A leukocyte disease characterized by autosomal dominant inheritance of lifelong, persistent elevated neutrophil counts primarily consisting of segmented neutrophils that has_material_basis_in heterozygous mutation in the colony stimulating factor 3 receptor (CSF3R) gene on chromosome 1p34."
    },
    "synonyms": [
        {
            "id": "MONDO:0008092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008092",
            "name": "hereditary neutrophilia",
            "description": "A leukocyte disease characterized by autosomal dominant inheritance of lifelong, persistent elevated neutrophil counts primarily consisting of segmented neutrophils that has material basis in heterozygous mutation in the CSF3R gene on chromosome 1p34."
        },
        {
            "id": "MIM:162830",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/162830",
            "name": "Hereditary neutrophilia",
            "description": "Hereditary neutrophilia"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0090120"
    ],
    "unlinked_id_list": []
}