{
    "disease_id": "DOID:0080237",
    "recommended_name": {
        "id": "DOID:0080237",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080237",
        "name": "autosomal dominant mental retardation 46",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in heterozygous mutation in the KCNQ5 gene on chromosome 6q14."
    },
    "synonyms": [
        {
            "id": "MONDO:0030911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030911",
            "name": "intellectual disability, autosomal dominant 46",
            "description": ""
        },
        {
            "id": "MONDO:0030911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030911",
            "name": "autosomal dominant mental retardation 46",
            "description": ""
        },
        {
            "id": "MONDO:0030911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030911",
            "name": "MRD46",
            "description": ""
        },
        {
            "id": "MONDO:0030911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030911",
            "name": "mental retardation, autosomal dominant 46",
            "description": ""
        },
        {
            "id": "MONDO:0030911",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030911",
            "name": "mental retardation, autosomal dominant 46; MRD46",
            "description": ""
        },
        {
            "id": "MIM:617601",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617601",
            "name": "Intellectual developmental disorder, autosomal dominant 46",
            "description": "Intellectual developmental disorder, autosomal dominant 46"
        }
    ]
}