{
    "disease_id": "DOID:0090012", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011225", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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            "id": "MONDO:0011225", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "severe combined immunodeficiency, Athabascan type"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "severe combined immunodeficiency, Athabaskan-type"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionizing radiation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "DCLRE1C severe combined immunodeficiency (disease)"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
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        {
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "SCID, Athabascan type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011225", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011225", 
            "name": "severe combined immunodeficiency, partial"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "Severe combined immunodeficiency due to artemis deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "SCID due to DCLRE1C deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "SCID due to artemis deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "SCID, Athabascan type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "SCID, Athabaskan type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "Severe combined immunodeficiency, Athabascan type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "Severe combined immunodeficiency, Athabaskan type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "artemis deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090012", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090012", 
            "name": "Severe combined immunodeficiency due to DCLRE1C deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090012", 
        "description": "A severe combined immunodeficiency characterized by being T cell-negative, B cell-negative and natural killer cell-positive with sensitivity to ionizing radiation and that has_material_basis_in mutation in the DCLRE1C gene on chromosome 10p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090012", 
        "name": "severe combined immunodeficiency with sensitivity to ionizing radiation"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090012#disease-associations", 
            "id": "0090012", 
            "database": "Alliance of Genome Resources"
        }
    ]
}