{
    "disease_id": "DOID:0070071",
    "recommended_name": {
        "id": "DOID:0070071",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070071",
        "name": "autosomal dominant intellectual developmental disorder 41",
        "description": "An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TBL1XR1 gene on chromosome 3q26.32."
    },
    "synonyms": [
        {
            "id": "DOID:0070071",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070071",
            "name": "autosomal dominant non-syndromic intellectual disability 41",
            "description": ""
        },
        {
            "id": "DOID:0070071",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070071",
            "name": "MRD41",
            "description": ""
        },
        {
            "id": "DOID:0070071",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070071",
            "name": "autosomal dominant mental retardation 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "intellectual disability, autosomal dominant 41",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the TBL1XR1 gene."
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "MRD41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "TBL1XR1 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "autosomal dominant intellectual disability 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "autosomal dominant mental retardation 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "intellectual disability, autosomal dominant 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "intellectual disability, autosomal dominant type 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "mental retardation, autosomal dominant 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "mental retardation, autosomal dominant type 41",
            "description": ""
        },
        {
            "id": "MONDO:0014842",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014842",
            "name": "autosomal dominant non-syndromic intellectual disability 41",
            "description": ""
        },
        {
            "id": "MIM:616944",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/616944",
            "name": "Intellectual developmental disorder, autosomal dominant 41",
            "description": "Intellectual developmental disorder, autosomal dominant 41"
        }
    ]
}