{
    "disease_id": "DOID:0060765", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "autosomal dominant Robinow syndrome caused by mutation in DVL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "Robinow syndrome, autosomal dominant 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "DRS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "DVL1 autosomal dominant Robinow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "Robinow syndrome, autosomal dominant type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "Robinow syndrome, autosomal dominant 2; DRS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014591", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014591", 
            "name": "autosomal dominant Robinow syndrome type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060765", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060765", 
            "name": "DRS2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060765", 
        "description": "A Robinow syndrome characterized by autosomal dominant inheritance of mesomelic limb shortening, genital hypoplasia, and distinctive facial features that has_material_basis_in heterozygous mutation in the DVL1 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060765", 
        "name": "autosomal dominant Robinow syndrome 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060765#disease-associations", 
            "id": "0060765", 
            "database": "Alliance of Genome Resources"
        }
    ]
}