{
    "disease_id": "DOID:0070044",
    "recommended_name": {
        "id": "DOID:0070044",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070044",
        "name": "Coffin-Siris syndrome 2",
        "description": "A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the ARID1A gene on chromosome 1p36.11."
    },
    "synonyms": [
        {
            "id": "DOID:0070044",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070044",
            "name": "CSS2",
            "description": ""
        },
        {
            "id": "DOID:0070044",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070044",
            "name": "MRD14",
            "description": ""
        },
        {
            "id": "DOID:0070044",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070044",
            "name": "autosomal dominant mental retardation 14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "intellectual disability, autosomal dominant 14",
            "description": "Any Coffin-Siris syndrome in which the cause of the disease is a mutation in the ARID1A gene."
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "ARID1A Coffin-Siris syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "ARID1A-related BAFopathy",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "CSS2",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "Coffin-Siris syndrome caused by mutation in ARID1A",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "MRD14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "autosomal dominant intellectual disability 14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "intellectual disability, autosomal dominant 14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "intellectual disability, autosomal dominant type 14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "mental retardation, autosomal dominant type 14",
            "description": ""
        },
        {
            "id": "MONDO:0013819",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013819",
            "name": "mental retardation, autosomal dominant 14",
            "description": ""
        },
        {
            "id": "MIM:614607",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614607",
            "name": "Coffin-Siris syndrome 2",
            "description": "Coffin-Siris syndrome 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070044"
    ],
    "unlinked_id_list": []
}