{
    "disease_id": "DOID:0081226",
    "recommended_name": {
        "id": "DOID:0081226",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081226",
        "name": "autosomal recessive intellectual developmental disorder 65",
        "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous or compound heterozygous mutation in the KDM5B gene on chromosome 1q32."
    },
    "synonyms": [
        {
            "id": "MONDO:0020850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020850",
            "name": "intellectual disability, autosomal recessive 65",
            "description": ""
        },
        {
            "id": "MONDO:0020850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020850",
            "name": "MRT65",
            "description": ""
        },
        {
            "id": "MONDO:0020850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020850",
            "name": "intellectual disability, autosomal recessive 65",
            "description": ""
        },
        {
            "id": "MONDO:0020850",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0020850",
            "name": "mental retardation, autosomal recessive 65",
            "description": ""
        },
        {
            "id": "MIM:618109",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/618109",
            "name": "Intellectual developmental disorder, autosomal recessive 65",
            "description": "Intellectual developmental disorder, autosomal recessive 65"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081226"
    ],
    "unlinked_id_list": []
}