{
    "disease_id": "DOID:0081190",
    "recommended_name": {
        "id": "DOID:0081190",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0081190",
        "name": "autosomal recessive intellectual developmental disorder 18",
        "description": "An autosomal recessive intellectual developmental disorder that is characterized by impaired intellectual development with or without epilepsy and that has_material_basis_in homozygous or compound heterozygous mutation in the MED23 gene on chromosome 6q23."
    },
    "synonyms": [
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "intellectual disability, autosomal recessive 18",
            "description": "Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the MED23 gene."
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MED23 autosomal recessive non-syndromic intellectual disability",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "autosomal recessive non-syndromic intellectual disability caused by mutation in MED23",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "intellectual developmental disorder, autosomal recessive 18, with or without epilepsy",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "intellectual disability, autosomal recessive 18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "intellectual disability, autosomal recessive type 18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "mental retardation, autosomal recessive type 18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MED23",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "MRT18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "autosomal recessive nonsyndromic intellectual disability-18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "autosomal recessive nonsyndromic mental retardation-18",
            "description": ""
        },
        {
            "id": "MONDO:0013651",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013651",
            "name": "mental retardation, autosomal recessive 18",
            "description": ""
        },
        {
            "id": "MIM:614249",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614249",
            "name": "Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy",
            "description": "Intellectual developmental disorder, autosomal recessive 18, with or without epilepsy"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0081190"
    ],
    "unlinked_id_list": []
}