{
    "disease_id": "DOID:0060819",
    "recommended_name": {
        "id": "DOID:0060819",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060819",
        "name": "syndromic X-linked intellectual disability Chudley-Schwartz type",
        "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has_material_basis_in variation in the chromosomal region Xq21.33-q23."
    },
    "synonyms": [
        {
            "id": "DOID:0060819",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060819",
            "name": "MRXSCS",
            "description": ""
        },
        {
            "id": "DOID:0060819",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060819",
            "name": "mental retardation, X-linked, syndromic, Chudley-Schwartz type",
            "description": ""
        },
        {
            "id": "DOID:0060819",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060819",
            "name": "X-linked mental retardation with seizures, hypogammaglobinemia, and gait disturbance",
            "description": ""
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "syndromic X-linked intellectual disability Chudley-Schwartz type",
            "description": "A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has_material_basis_in variation in the chromosomal region Xq21.33-q23."
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "MRXSCS",
            "description": ""
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "mental retardation, X-linked, syndromic, Chudley-Schwartz type; MRXSCS",
            "description": ""
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "X-linked mental retardation with seizures, hypogammaglobinemia, and gait disturbance",
            "description": ""
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "mental retardation, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance",
            "description": ""
        },
        {
            "id": "MONDO:0010462",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010462",
            "name": "mental retardation, X-linked, syndromic, Chudley-Schwartz type",
            "description": ""
        }
    ]
}