{
    "disease_id": "DOID:0060828",
    "recommended_name": {
        "id": "DOID:0060828",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0060828",
        "name": "X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome",
        "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, delayed psychomotor development, seizures, large joint contractures, cardiac abnormalities, and abnormal positioning of the thumbs that has_material_basis_in mutation in the CLIC2 gene on chromosome Xq28."
    },
    "synonyms": [
        {
            "id": "DOID:0060828",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060828",
            "name": "MRXS32",
            "description": ""
        },
        {
            "id": "DOID:0060828",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0060828",
            "name": "mental retardation, X-linked, syndromic 32",
            "description": ""
        },
        {
            "id": "MONDO:0010473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010473",
            "name": "X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome",
            "description": "A syndromic X-linked intellectual disability characterized by intellectual disability, delayed psychomotor development, seizures, large joint contractures, cardiac abnormalities, and abnormal positioning of the thumbs that has_material_basis_in mutation in the CLIC2 gene on chromosome Xq28."
        },
        {
            "id": "MONDO:0010473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010473",
            "name": "MRXS32",
            "description": ""
        },
        {
            "id": "MONDO:0010473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010473",
            "name": "mental retardation, X-linked, syndromic type 32",
            "description": ""
        },
        {
            "id": "MONDO:0010473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010473",
            "name": "mental retardation, X-linked, syndromic 32; MRXS32",
            "description": ""
        },
        {
            "id": "MONDO:0010473",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010473",
            "name": "mental retardation, X-linked, syndromic 32",
            "description": ""
        },
        {
            "id": "MIM:300886",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300886",
            "name": "Intellectual developmental disorder, X-linked, syndromic 32",
            "description": "Intellectual developmental disorder, X-linked, syndromic 32"
        }
    ]
}