{
    "disease_id": "DOID:0112128", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "neutropenia, severe congenital, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "Xln"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "severe congenital neutropenia X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "SCNX"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "severe congenital neutropenia, X-linked"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010294", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010294", 
            "name": "neutropenia, severe congenital, X-linked; SCNX"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112128", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112128", 
            "name": "XLN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112128", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112128", 
            "name": "SCNX"
        }, 
        {
            "url": "https://www.omim.org/entry/300299", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:300299", 
            "name": "Neutropenia, severe congenital, X-linked"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112128", 
        "description": "A severe congenital neutropenia that has_material_basis_in hemizygous activating mutation in WAS on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112128", 
        "name": "X-linked severe congenital neutropenia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300299", 
            "id": "300299", 
            "database": "MIM"
        }
    ]
}