{
    "disease_id": "DOID:0070034",
    "recommended_name": {
        "id": "DOID:0070034",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070034",
        "name": "autosomal dominant non-syndromic intellectual disability 4",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of KIRREL3 on chromosome 11q24.2."
    },
    "synonyms": [
        {
            "id": "DOID:0070034",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070034",
            "name": "MRD4",
            "description": ""
        },
        {
            "id": "DOID:0070034",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070034",
            "name": "autosomal dominant mental retardation 4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "intellectual disability, autosomal dominant 4",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the KIRREL3 gene."
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "autosomal dominant non-syndromic intellectual disability 4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "autosomal dominant mental retardation 4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in KIRREL3",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "mental retardation, autosomal dominant type 4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "mental retardation, autosomal dominant 4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "mental retardation, autosomal dominant 4; MRD4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "MRD4",
            "description": ""
        },
        {
            "id": "MONDO:0012947",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012947",
            "name": "KIRREL3 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        }
    ]
}