{
    "disease_id": "DOID:0080239",
    "recommended_name": {
        "id": "DOID:0080239",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080239",
        "name": "autosomal recessive intellectual developmental disorder 61",
        "description": "An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the RUN and SH3 domain containing 2 gene (RUSC2) on chromosome 9p13."
    },
    "synonyms": [
        {
            "id": "DOID:0080239",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080239",
            "name": "Alwadei syndrome",
            "description": ""
        },
        {
            "id": "DOID:0080239",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080239",
            "name": "autosomal recessive intellectual developmental disorder-61",
            "description": ""
        },
        {
            "id": "DOID:0080239",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080239",
            "name": "autosomal recessive mental retardation 61",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "intellectual disability, autosomal recessive 61",
            "description": "An autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13."
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "intellectual disability, autosomal recessive 61",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "Alwadei syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "MRT61",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "autosomal recessive intellectual disability 61",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "autosomal recessive mental retardation 61",
            "description": ""
        },
        {
            "id": "MONDO:0030915",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0030915",
            "name": "mental retardation, autosomal recessive 61",
            "description": ""
        },
        {
            "id": "MIM:617773",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617773",
            "name": "Intellectual developmental disorder, autosomal recessive 61",
            "description": "Intellectual developmental disorder, autosomal recessive 61"
        }
    ]
}
