{
    "disease_id": "DOID:0081227",
    "recommended_name": {
        "id": "DOID:0081227",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081227",
        "name": "autosomal recessive intellectual developmental disorder 66",
        "description": "An autosomal recessive intellectual developmental disorder that is characterized by delayed speech development, neuropsychiatric symptoms, and relatively normal life span and that has_material_basis_in homozygous mutation in the C12ORF4 gene on chromosome 12p13."
    },
    "synonyms": [
        {
            "id": "MONDO:0032605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032605",
            "name": "intellectual disability, autosomal recessive 66",
            "description": ""
        },
        {
            "id": "MONDO:0032605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032605",
            "name": "intellectual developmental disorder, autosomal recessive 66",
            "description": ""
        },
        {
            "id": "MONDO:0032605",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0032605",
            "name": "MRT66",
            "description": ""
        },
        {
            "id": "MIM:618221",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618221",
            "name": "Intellectual developmental disorder, autosomal recessive 66",
            "description": "Intellectual developmental disorder, autosomal recessive 66"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081227"
    ],
    "unlinked_id_list": []
}