{
    "disease_id": "DOID:0060227",
    "recommended_name": {
        "id": "DOID:0060227",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060227",
        "name": "Adams-Oliver syndrome",
        "description": "A syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs."
    },
    "synonyms": [
        {
            "id": "DOID:0060227",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0060227",
            "name": "Adams Oliver syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "Adams-Oliver syndrome 2",
            "description": "Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the DOCK6 gene."
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "Adams-Oliver syndrome 2",
            "description": ""
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "Adams-Oliver syndrome caused by mutation in DOCK6",
            "description": ""
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "Adams-Oliver syndrome type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "DOCK6 Adams-Oliver syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013635",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013635",
            "name": "AOS2",
            "description": ""
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "Adams-Oliver syndrome 4",
            "description": "Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the EOGT gene."
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "Adams-Oliver syndrome 4",
            "description": ""
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "Adams-Oliver syndrome caused by mutation in EOGT",
            "description": ""
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "Adams-Oliver syndrome type 4",
            "description": ""
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "EOGT Adams-Oliver syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014124",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014124",
            "name": "AOS4",
            "description": ""
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "Adams-Oliver syndrome 5",
            "description": "Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the NOTCH1 gene."
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "AOS5",
            "description": ""
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "Adams-Oliver syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "Adams-Oliver syndrome caused by mutation in NOTCH1",
            "description": ""
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "Adams-Oliver syndrome caused by mutation in Notch1",
            "description": ""
        },
        {
            "id": "MONDO:0014459",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014459",
            "name": "Adams-Oliver syndrome type 5",
            "description": ""
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "Adams-Oliver syndrome 1",
            "description": "Any Adams-Oliver syndrome in which the cause of the disease is a mutation in the ARHGAP31 gene."
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "AOS1",
            "description": ""
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "ARHGAP31 Adams-Oliver syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "Adams-Oliver syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "Adams-Oliver syndrome caused by mutation in ARHGAP31",
            "description": ""
        },
        {
            "id": "MONDO:0024506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0024506",
            "name": "AOS",
            "description": ""
        },
        {
            "id": "MIM:614219",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614219",
            "name": "Adams-Oliver syndrome 2",
            "description": "Adams-Oliver syndrome 2"
        },
        {
            "id": "MIM:615297",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615297",
            "name": "Adams-Oliver syndrome 4",
            "description": "Adams-Oliver syndrome 4"
        },
        {
            "id": "MIM:616028",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616028",
            "name": "Adams-Oliver syndrome 5",
            "description": "Adams-Oliver syndrome 5"
        },
        {
            "id": "MIM:100300",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/100300",
            "name": "Adams-Oliver syndrome 1",
            "description": "Adams-Oliver syndrome 1"
        }
    ],
    "children": [
        {
            "id": "DOID:0061179",
            "label": "Adams-Oliver syndrome 3",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0060227",
        "DOID:0061179"
    ],
    "unlinked_id_list": []
}