{
    "disease_id": "DOID:0111971", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "CD3-Epsilon deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "immunodeficiency 18, SCID variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "IMD18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "immunodeficiency 18; IMD18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "immunodeficiency 18, Severe combined immunodeficiency variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014278", 
            "name": "immunodeficiency type 18"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111971", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111971", 
            "name": "CD3-epsilon deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111971", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111971", 
            "name": "IMD18"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111971", 
        "description": "A primary immunodeficiency disease characterized by onset in infancy or early childhood of recurrent infections with variable severity that has_material_basis_in homozygous or compound heterozygous mutation in CD3E on chromosome 11q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111971", 
        "name": "immunodeficiency 18"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615615", 
            "id": "615615", 
            "database": "MIM"
        }
    ]
}