{
    "disease_id": "DOID:0070052",
    "recommended_name": {
        "id": "DOID:0070052",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070052",
        "name": "autosomal dominant non-syndromic intellectual disability 22",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of ZBTB18 on chromosome 1q44."
    },
    "synonyms": [
        {
            "id": "DOID:0070052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070052",
            "name": "MRD22",
            "description": ""
        },
        {
            "id": "DOID:0070052",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070052",
            "name": "autosomal dominant mental retardation 22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "intellectual disability, autosomal dominant 22",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the ZBTB18 gene."
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "chromosome 1Q43-q44 deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "mental retardation, autosomal dominant 22; MRD22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "MRD22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "chromosome 1Qter deletion syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "autosomal dominant non-syndromic intellectual disability 22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "mental retardation, autosomal dominant 22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "ZBTB18 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "autosomal dominant mental retardation 22",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18",
            "description": ""
        },
        {
            "id": "MONDO:0012869",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012869",
            "name": "mental retardation, autosomal dominant type 22",
            "description": ""
        },
        {
            "id": "MIM:612337",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612337",
            "name": "Intellectual developmental disorder, autosomal dominant 22",
            "description": "Intellectual developmental disorder, autosomal dominant 22"
        }
    ]
}