{
    "disease_id": "DOID:1919",
    "recommended_name": {
        "id": "DOID:1919",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1919",
        "name": "Lesch-Nyhan syndrome",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "Hypoxanthine-guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "HG-PRT deficiency",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "Lesch - Nyhan syndrome",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "X-linked hyperuricemia",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "deficiency of IMP pyrophosphorylase",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "Complete hypoxanthine-guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "DOID:1919",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1919",
            "name": "Hypoxanthine-guanine-phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch-Nyhan syndrome",
            "description": "Lesch-Nyhan syndrome (LNS) is the most severe form of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency (see this term), a hereditary disorder of purine metabolism, and is associated with uric acid overproduction (UAO), neurological troubles, and behavioral problems."
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch Nyhan disease",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HPRT deficiency, complete",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "LNS",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "complete hypoxanthine-guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HPRT deficiency, neurologic variant",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine guanine phosphoribosyltransferase 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "X-linked hyperuricemia",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine guanine phosphoribosyltransferase complete deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch-Nyhan syndrome; LNS",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HPRT complete deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "deficiency of IMP pyrophosphorylase",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "X-linked hyperuricemia (disorder) [ambiguous]",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch - Nyhan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch-Nyhan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HPRT deficiency grade IV",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine guanine phospho-ribosyltransferase 1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder) [ambiguous]",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine-guanine phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Hprt1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch-Nyhan syndrome, neurologic variant",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HG-PRT deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "HPRT deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "Lesch Nyhan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010298",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010298",
            "name": "hypoxanthine-guanine-phosphoribosyltransferase deficiency",
            "description": ""
        },
        {
            "id": "MIM:300322",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300322",
            "name": "Lesch-Nyhan syndrome",
            "description": "Lesch-Nyhan syndrome"
        }
    ]
}