{
    "disease_id": "DOID:0112370",
    "recommended_name": {
        "id": "DOID:0112370",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112370",
        "name": "Coffin-Siris syndrome 12",
        "description": "A Coffin-Siris syndrome characterized by global developmental delay with variably impaired intellectual development, speech and language delay, and behavioral abnormalities, such as autism or hyperactivity that has_material_basis_in heterozygous mutation in the BICRA gene on chromosome 19q13.33."
    },
    "synonyms": [
        {
            "id": "DOID:0112370",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112370",
            "name": "CSS12",
            "description": ""
        },
        {
            "id": "MONDO:0025699",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0025699",
            "name": "Coffin-Siris syndrome 12",
            "description": ""
        },
        {
            "id": "MONDO:0025699",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0025699",
            "name": "CSS12",
            "description": ""
        },
        {
            "id": "MIM:619325",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/619325",
            "name": "Coffin-Siris syndrome 12",
            "description": "Coffin-Siris syndrome 12"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112370"
    ],
    "unlinked_id_list": []
}