{
    "disease_id": "DOID:0070048",
    "recommended_name": {
        "id": "DOID:0070048",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070048",
        "name": "autosomal dominant non-syndromic intellectual disability 18",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3."
    },
    "synonyms": [
        {
            "id": "DOID:0070048",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070048",
            "name": "MRD18",
            "description": ""
        },
        {
            "id": "DOID:0070048",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070048",
            "name": "autosomal dominant mental retardation 18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome",
            "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of GATAD2B on chromosome 1q21.3."
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "mental retardation, autosomal dominant type 18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "GATAD2B-associated neurodevelopmental disorder",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "autosomal dominant mental retardation 18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "mental retardation, autosomal dominant 18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "autosomal dominant non-syndromic intellectual disability 18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "mental retardation, autosomal dominant 18; MRD18",
            "description": ""
        },
        {
            "id": "MONDO:0014034",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014034",
            "name": "MRD18",
            "description": ""
        },
        {
            "id": "MIM:615074",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615074",
            "name": "Gand syndrome",
            "description": "Gand syndrome"
        }
    ]
}