{
    "disease_id": "DOID:0070069", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "intellectual disability, autosomal dominant 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "chromosome 2P25.3 Duplication syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "chromosome 2P25.3 deletion syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "mental retardation, autosomal dominant 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "mental retardation, autosomal dominant 39; MRD39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "autosomal dominant mental retardation 39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "MRD39"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "MYT1L autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014678", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014678", 
            "name": "mental retardation, autosomal dominant type 39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070069", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070069", 
            "name": "MRD39"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070069", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070069", 
            "name": "autosomal dominant mental retardation 39"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070069", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070069", 
        "name": "autosomal dominant non-syndromic intellectual disability 39"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070069#disease-associations", 
            "id": "0070069", 
            "database": "Alliance of Genome Resources"
        }
    ]
}