{
    "disease_id": "DOID:2962", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "Cockayne syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "Cockayne syndrome B; CSB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "CSB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "Cockayne syndrome type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "Cockayne syndrome B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019570", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019570", 
            "name": "Cockayne syndrome type B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2962", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2962", 
            "name": "Neill-Dingwall syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2962", 
        "description": "A syndrome that has_material_basis_in rare mutations in two DNA excision repair proteins, ERCC-8 and ERCC-6, and characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), and premature aging.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2962", 
        "name": "Cockayne syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2962#disease-associations", 
            "id": "2962", 
            "database": "Alliance of Genome Resources"
        }
    ]
}