{
    "disease_id": "DOID:0080232",
    "recommended_name": {
        "id": "DOID:0080232",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080232",
        "name": "autosomal dominant intellectual developmental disorder 51",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KMT5B gene on chromosome 11q13."
    },
    "synonyms": [
        {
            "id": "DOID:0080232",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080232",
            "name": "autosomal dominant mental retardation 51",
            "description": ""
        },
        {
            "id": "MONDO:0030917",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030917",
            "name": "intellectual disability, autosomal dominant 51",
            "description": ""
        },
        {
            "id": "MONDO:0030917",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030917",
            "name": "intellectual disability, autosomal dominant 51",
            "description": ""
        },
        {
            "id": "MONDO:0030917",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030917",
            "name": "MRD51",
            "description": ""
        },
        {
            "id": "MONDO:0030917",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030917",
            "name": "autosomal dominant mental retardation 51",
            "description": ""
        },
        {
            "id": "MONDO:0030917",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030917",
            "name": "mental retardation, autosomal dominant 51",
            "description": ""
        },
        {
            "id": "MIM:617788",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617788",
            "name": "Intellectual developmental disorder, autosomal dominant 51",
            "description": "Intellectual developmental disorder, autosomal dominant 51"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080232"
    ],
    "unlinked_id_list": []
}