{
    "disease_id": "DOID:0060020", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "DeVaal disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "RD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "generalized hematopoietic hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "aleukocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "reticular Dysgenesia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "hematopoietic hypoplasia, generalized"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "SCID with leukopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "severe combined immunodeficiency with leukopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "congenital aleukocytosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "De Vaal disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "AK2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009973", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009973", 
            "name": "congenital Aleukia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060020", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060020", 
            "name": "De Vaal disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060020", 
        "description": "A severe combined immunodeficiency that is the most severe form of SCID and has_material_basis_in mutations in the gene encoding mitochondrial adenylate kinase 2. It is characterized by congenital agranulocytosis, lymphopenia, and lymphoid and thymic hypoplasia with absent cellular and humoral immunity functions.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060020", 
        "name": "reticular dysgenesis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060020#disease-associations", 
            "id": "0060020", 
            "database": "Alliance of Genome Resources"
        }
    ]
}