{
    "disease_id": "DOID:0090120",
    "recommended_name": {
        "id": "DOID:0090120",
        "resource": "Disease Ontology",
        "url": "http://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": "MONDO:0008092",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008092",
            "name": "neutrophilia, hereditary",
            "description": ""
        },
        {
            "id": "MIM:162830",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/162830",
            "name": "Hereditary neutrophilia",
            "description": "Hereditary neutrophilia"
        }
    ]
}