{
    "disease_id": "DOID:0060767",
    "recommended_name": {
        "id": "DOID:0060767",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060767",
        "name": "autosomal dominant Robinow syndrome 3",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0060767",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060767",
            "name": "DRS3",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "autosomal dominant Robinow syndrome 3",
            "description": "Any Robinow syndrome in which the cause of the disease is a mutation in the DVL3 gene."
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "DRS3",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "DVL3 Robinow syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "Robinow syndrome caused by mutation in DVL3",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "Robinow syndrome, autosomal dominant 3",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "Robinow syndrome, autosomal dominant type 3",
            "description": ""
        },
        {
            "id": "MONDO:0014819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014819",
            "name": "autosomal dominant Robinow syndrome type 3",
            "description": ""
        },
        {
            "id": "MIM:616894",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616894",
            "name": "Robinow syndrome, autosomal dominant 3",
            "description": "Robinow syndrome, autosomal dominant 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060767"
    ],
    "unlinked_id_list": []
}