{
    "disease_id": "DOID:0070069",
    "recommended_name": {
        "id": "DOID:0070069",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070069",
        "name": "autosomal dominant intellectual developmental disorder 39",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070069",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070069",
            "name": "MRD39",
            "description": ""
        },
        {
            "id": "DOID:0070069",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070069",
            "name": "autosomal dominant mental retardation 39",
            "description": ""
        },
        {
            "id": "DOID:0070069",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070069",
            "name": "autosomal dominant non-syndromic intellectual disability 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "intellectual disability, autosomal dominant 39",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MYT1L gene."
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "MRD39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "MYT1L autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "autosomal dominant intellectual disability 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "intellectual developmental disorder, autosomal dominant 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "intellectual disability, autosomal dominant 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "intellectual disability, autosomal dominant type 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "mental retardation, autosomal dominant type 39",
            "description": ""
        },
        {
            "id": "MONDO:0014678",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014678",
            "name": "mental retardation, autosomal dominant 39",
            "description": ""
        },
        {
            "id": "MIM:616521",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616521",
            "name": "Intellectual developmental disorder, autosomal dominant 39",
            "description": "Intellectual developmental disorder, autosomal dominant 39"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070069"
    ],
    "unlinked_id_list": []
}