{
    "disease_id": "DOID:14731", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "EZH2 related overgrowth"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "WEAVER syndrome; WVS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "WVS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver-like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver-Williams syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver Smith syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver-Smith syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "camptodactyly-overgrowth-unusual facies syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver like syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "Weaver Williams syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "mental retardation, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010193", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010193", 
            "name": "camptodactyly - overgrowth - unusual facies"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14731", 
            "name": "WEAVER-LIKE SYNDROME"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14731", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14731", 
            "name": "Weaver-Williams syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14731", 
        "description": "A syndrome that is characterized by prenatal and postnatal overgrowth, accelerated osseous maturation, characteristic craniofacial appearance, and developmental delay and has_material_basis_in heterozygous mutation in the EZH2 gene on chromosome 7q36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14731", 
        "name": "Weaver syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14731#disease-associations", 
            "id": "14731", 
            "database": "Alliance of Genome Resources"
        }
    ]
}