{
    "disease_id": "DOID:0081201",
    "recommended_name": {
        "id": "DOID:0081201",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0081201",
        "name": "autosomal recessive intellectual developmental disorder 35",
        "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 12.2-Mb region on chromosome 17q21.31-q22 between SNPs rs4792947 and rs11079258."
    },
    "synonyms": [
        {
            "id": "MONDO:0014067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014067",
            "name": "short ulna-dysmorphism-hypotonia-intellectual disability syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014067",
            "name": "MRT35",
            "description": ""
        },
        {
            "id": "MONDO:0014067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014067",
            "name": "intellectual disability, autosomal recessive 35",
            "description": ""
        },
        {
            "id": "MONDO:0014067",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014067",
            "name": "mental retardation, autosomal recessive 35",
            "description": ""
        }
    ]
}