{
    "disease_id": "DOID:0070071", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "intellectual disability, autosomal dominant 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "intellectual disability, autosomal dominant 41; MRD41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "MRD41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "autosomal dominant mental retardation 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "mental retardation, autosomal dominant type 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "mental retardation, autosomal dominant 41"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "TBL1XR1 autosomal dominant non-syndromic intellectual disability"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014842", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014842", 
            "name": "mental retardation, autosomal dominant 41; MRD41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070071", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070071", 
            "name": "MRD41"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070071", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070071", 
            "name": "autosomal dominant mental retardation 41"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070071", 
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of TBL1XR1 on chromosome 3q26.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070071", 
        "name": "autosomal dominant non-syndromic intellectual disability 41"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070071#disease-associations", 
            "id": "0070071", 
            "database": "Alliance of Genome Resources"
        }
    ]
}