{
    "disease_id": "DOID:0060019", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "severe combined immunodeficiency due to CORO1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "IMD8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "severe combined immunodeficiency due to coronin-1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "SCID due to coronin-1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "immunodeficiency 8; IMD8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "immunodeficiency 8"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "SCID due to CORO1A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014168", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014168", 
            "name": "immunodeficiency type 8"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060019", 
        "description": "A severe combined immunodeficiency that is an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060019", 
        "name": "coronin-1A deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060019#disease-associations", 
            "id": "0060019", 
            "database": "Alliance of Genome Resources"
        }
    ]
}