{
    "disease_id": "DOID:12960",
    "recommended_name": {
        "id": "DOID:12960",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:12960",
        "name": "acrocephalosyndactylia",
        "description": "A synostosis that results_in craniosynostosis and syndactyly."
    },
    "synonyms": [
        {
            "id": "DOID:12960",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:12960",
            "name": "Apert syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "apert syndrome",
            "description": "Apert syndrome (AS) is a frequent form of acrocephalosyndactyly (see this term), a group of inherited congenital malformation disorders, characterized by craniosynostosis (see this term), midface hypoplasia, and finger and toe anomalies and/or syndactyly."
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "syndactylic oxycephaly",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "type I Acrocephalosyndactyly",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "ACS 2",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "ACS 1",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "acrocephalosyndactyly type I",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "apert syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "acrocephalo-syndactyly type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "ACS1",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "acrocephalosyndactyly, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "apert-Crouzon disease",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "acrocephalosyndactyly type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "acrocephalosyndactyly, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007041",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007041",
            "name": "Vogt Cephalodactyly",
            "description": ""
        },
        {
            "id": "MIM:101200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/101200",
            "name": "Apert syndrome",
            "description": "Apert syndrome"
        }
    ]
}