{
    "disease_id": "DOID:0080232", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030917", 
            "name": "intellectual disability, autosomal dominant 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030917", 
            "name": "MRD51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030917", 
            "name": "mental retardation, autosomal dominant 51"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0030917", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0030917", 
            "name": "mental retardation, autosomal dominant 51; MRD51"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080232", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in heterozygous mutation in the KMT5B gene on chromosome 11q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080232", 
        "name": "autosomal dominant mental retardation 51"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080232#disease-associations", 
            "id": "0080232", 
            "database": "Alliance of Genome Resources"
        }
    ]
}