{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "adult progeria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "WRN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "Werner's syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "Werner syndrome; WRN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "WS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010196", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010196", 
            "name": "adult premature ageing syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:5688", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:5688", 
            "name": "WS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:5688", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:5688", 
            "name": "Werner's syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:5688", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:5688", 
            "name": "adult premature ageing syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:5688", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:5688", 
            "name": "adult progeria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:5688", 
        "description": "A syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.", 
        "resource": "Disease Ontology", 
        "id": "DOID:5688", 
        "name": "Werner syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277700", 
            "id": "277700", 
            "database": "MIM"
        }
    ]
}