{
    "disease_id": "DOID:0080231",
    "recommended_name": {
        "id": "DOID:0080231",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080231",
        "name": "autosomal dominant mental retardation 52",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in heterozygous mutation in the ASH1L gene on chromosome 1q22."
    },
    "synonyms": [
        {
            "id": "MONDO:0030918",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030918",
            "name": "intellectual disability, autosomal dominant 52",
            "description": ""
        },
        {
            "id": "MONDO:0030918",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030918",
            "name": "autosomal dominant mental retardation 52",
            "description": ""
        },
        {
            "id": "MONDO:0030918",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030918",
            "name": "mental retardation, autosomal dominant 52; MRD52",
            "description": ""
        },
        {
            "id": "MONDO:0030918",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030918",
            "name": "MRD52",
            "description": ""
        },
        {
            "id": "MONDO:0030918",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030918",
            "name": "mental retardation, autosomal dominant 52",
            "description": ""
        },
        {
            "id": "MIM:617796",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617796",
            "name": "Intellectual developmental disorder, autosomal dominant 52",
            "description": "Intellectual developmental disorder, autosomal dominant 52"
        }
    ]
}