{
    "disease_id": "DOID:0060307", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "intellectual disability, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in MBD5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "mental retardation, autosomal dominant 1; MRD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "autosomal dominant mental retardation 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "autosomal dominant non-syndromic intellectual disability 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "mental retardation, autosomal dominant type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "chromosome 2Q23.1 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "MBD5 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "mental retardation, autosomal dominant 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007974", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007974", 
            "name": "MRD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060307", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060307", 
            "name": "autosomal dominant mental retardation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060307", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060307", 
            "name": "autosomal dominant non-syndromic mental retardation"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060307", 
        "description": "A non-syndromic intellectual disability characterized by an autosomal dominant inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060307", 
        "name": "autosomal dominant non-syndromic intellectual disability"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060307#disease-associations", 
            "id": "0060307", 
            "database": "Alliance of Genome Resources"
        }
    ]
}