{
    "disease_id": "DOID:11983", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader-Willi-Labhart syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Willi-Prader syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "PWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader-Willi-like syndrome associated with chromosome 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader-Labhart-Willi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader-Willi syndrome; PWS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader Willi syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008300", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008300", 
            "name": "Prader-Willi syndrome chromosome region"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:11983", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:11983", 
            "name": "Prader Willi syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:11983", 
        "description": "A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity.", 
        "resource": "Disease Ontology", 
        "id": "DOID:11983", 
        "name": "Prader-Willi syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/11983#disease-associations", 
            "id": "11983", 
            "database": "Alliance of Genome Resources"
        }
    ]
}