{
    "disease_id": "DOID:12798",
    "recommended_name": {
        "id": "DOID:12798",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:12798",
        "name": "mucopolysaccharidosis",
        "description": "A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine."
    },
    "synonyms": [
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "Hurler syndrome",
            "description": "Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS1; see this term), a rare lysosomal storage disease, characterized by skeletal abnormalities, cognitive impairment, heart disease, respiratory problems, enlarged liver and spleen, characteristic facies and reduced life expectancy."
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "mucopolysaccharidosis type IH",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "mucopolysaccharidosis type 1H",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "MPS1H",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "Hurler syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "Hurler disease",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "MPS1-H",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "MPSIH",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "mucopolysaccharidosis IH",
            "description": ""
        },
        {
            "id": "MONDO:0011758",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011758",
            "name": "MPS I H",
            "description": ""
        },
        {
            "id": "MONDO:0009654",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009654",
            "name": "mucopolysaccharidoses, unclassified types",
            "description": ""
        },
        {
            "id": "MONDO:0009654",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009654",
            "name": "mucopolysaccharidoses, unclassified types",
            "description": ""
        },
        {
            "id": "MIM:607014",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607014",
            "name": "Mucopolysaccharidosis 1H",
            "description": "Mucopolysaccharidosis 1H"
        }
    ]
}