{
    "disease_id": "DOID:0070035",
    "recommended_name": {
        "id": "DOID:0070035",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070035",
        "name": "autosomal dominant non-syndromic intellectual disability 5",
        "description": "An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of SYNGAP1 on chromosome 6p21.32."
    },
    "synonyms": [
        {
            "id": "DOID:0070035",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070035",
            "name": "MRD5",
            "description": ""
        },
        {
            "id": "DOID:0070035",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070035",
            "name": "autosomal dominant mental retardation 5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "intellectual disability, autosomal dominant 5",
            "description": "Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the SYNGAP1 gene."
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "SYNGAP1-related NSID",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "SYNGAP1 syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "SYNGAP1-related non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "mental retardation, autosomal dominant type 5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "mental retardation, autosomal dominant 5; MRD5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "autosomal dominant non-syndromic intellectual disability 5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "autosomal dominant mental retardation 5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "mental retardation, autosomal dominant 5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "SYNGAP1 autosomal dominant non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "MRD5",
            "description": ""
        },
        {
            "id": "MONDO:0012960",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012960",
            "name": "SYNGAP1 Gene mutation linked to intellectual disability, schizophrenia and autism",
            "description": ""
        },
        {
            "id": "MIM:612621",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/612621",
            "name": "Intellectual developmental disorder, autosomal dominant 5",
            "description": "Intellectual developmental disorder, autosomal dominant 5"
        }
    ]
}