{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "Robinow syndrome, autosomal dominant 3; DRS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "DRS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "Robinow syndrome caused by mutation in DVL3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "DVL3 Robinow syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "Robinow syndrome, autosomal dominant type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "autosomal dominant Robinow syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014819", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014819", 
            "name": "Robinow syndrome, autosomal dominant 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060767", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060767", 
            "name": "DRS3"
        }, 
        {
            "url": "https://www.omim.org/entry/616894", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:616894", 
            "name": "Robinow syndrome, autosomal dominant 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060767", 
        "description": "A Robinow syndrome characterized by autosomal dominant inheritance of mesomelia, genital hypoplasia, and distinctive facial features comprising frontal bossing, prominent eyes, and a depressed nasal bridge that has_material_basis_in heterozygous mutation in the DVL3 gene on chromosome 3q27.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060767", 
        "name": "autosomal dominant Robinow syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/616894", 
            "id": "616894", 
            "database": "MIM"
        }
    ]
}