{
    "disease_id": "DOID:0060238",
    "recommended_name": {
        "id": "DOID:0060238",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060238",
        "name": "Van Maldergem syndrome",
        "description": "A syndrome characterized by facial abnormalities such as telecanthus, epicanthus, broad flattened nose, large inverted W-shaped mouth and malformed ears, malformed extremities such as camptodactyly, clinodactyly, interdigital webbing and joint hyperlaxity and mental retardation."
    },
    "synonyms": [
        {
            "id": "DOID:0060238",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060238",
            "name": "cerebro-facio-articular syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "van Maldergem syndrome 1",
            "description": "Any van Maldergem syndrome in which the cause of the disease is a mutation in the DCHS1 gene."
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "DCHS1 van Maldergem syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "Van Maldergem syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "van Maldergem syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "van Maldergem syndrome caused by mutation in DCHS1",
            "description": ""
        },
        {
            "id": "MONDO:0011070",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011070",
            "name": "VMLDS1",
            "description": ""
        },
        {
            "id": "MIM:601390",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/601390",
            "name": "Van Maldergem syndrome 1",
            "description": "Van Maldergem syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0080585",
            "label": "Van Maldergem syndrome 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0080586",
            "label": "Van Maldergem syndrome 2",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0080585",
        "DOID:0080586",
        "DOID:0060238"
    ],
    "unlinked_id_list": []
}