{
    "disease_id": "DOID:0112064", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011988", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011988", 
            "name": "neutrophil immunodeficiency syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112064", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112064", 
            "name": "IMD73A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112064", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112064", 
            "name": "neutrophil immunodeficiency syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/608203", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:608203", 
            "name": "Neutrophil immunodeficiency syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112064", 
        "description": "A combined immunodeficiency characterized by onset of recurrent infections in early infancy, leukocytosis, neutrophilia, decreased TCR excision circles, decreased neutrophil chemotaxis, and T-cell abnormalities that has_material_basis_in heterozygous loss of function mutation in RAC2 on chromosome 22q13.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112064", 
        "name": "immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/608203", 
            "id": "608203", 
            "database": "MIM"
        }
    ]
}