{
    "disease_id": "DOID:0112038",
    "recommended_name": {
        "id": "DOID:0112038",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112038",
        "name": "non-syndromic X-linked intellectual disability 1",
        "description": "A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability in males and varying levels of intellectual disability in females that has_material_basis_in hemizygous or heterozygous mutation in the IQSEC2 gene on chromosome Xp11.22."
    },
    "synonyms": [
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "MRX1",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "MRX18",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "MRX78",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "X-linked mental retardation 1",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "X-linked mental retardation 1/78",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "X-linked mental retardation 18",
            "description": ""
        },
        {
            "id": "DOID:0112038",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112038",
            "name": "X-linked mental retardation 78",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "intellectual disability, X-linked 1",
            "description": "An X-linked dominant condition caused by mutation(s) in the IQSEC2 gene, encoding IQ motif and SEC7 domain-containing protein 2. It is characterized by substantially impaired intellectual functioning and behavioral abnormalities."
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "IQSEC2-related disorder",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "IQSEC2-related syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "MRX",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "MRX1",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "MRX78",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "intellectual developmental disorder, X-linked 1, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "intellectual disability, X-linked 1",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "mental retardation, X-linked 1",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "mental retardation, X-linked 18",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "mental retardation, X-linked 78",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "mental retardation, X-linked type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "IQSEC2",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "IQSEC2-related epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "IQSEC2-related intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "X-linked intellectual disability 1",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "X-linked intellectual disability 1/78",
            "description": ""
        },
        {
            "id": "MONDO:0010656",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010656",
            "name": "X-linked intellectual disability 78",
            "description": ""
        },
        {
            "id": "MIM:309530",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309530",
            "name": "Intellectual developmental disorder, X-linked 1",
            "description": "Intellectual developmental disorder, X-linked 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112038"
    ],
    "unlinked_id_list": []
}