{
    "disease_id": "DOID:1919", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HPRT deficiency, complete"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "LNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HPRT deficiency, neurologic variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine guanine phosphoribosyltransferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "X-linked hyperuricemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine guanine phosphoribosyltransferase complete deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "Lesch-Nyhan syndrome; LNS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HPRT complete deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "deficiency of IMP pyrophosphorylase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "X-linked hyperuricemia (disorder) [ambiguous]"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "Lesch - Nyhan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HPRT deficiency grade IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine guanine phospho-ribosyltransferase 1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder) [ambiguous]"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine-guanine phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "Hprt1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "Lesch-Nyhan syndrome, neurologic variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HG-PRT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "HPRT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "Lesch Nyhan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010298", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010298", 
            "name": "hypoxanthine-guanine-phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "Hypoxanthine-guanine phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "HG-PRT deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "Lesch - Nyhan syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "X-linked hyperuricemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "deficiency of IMP pyrophosphorylase"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "hypoxanthine guanine phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "Complete hypoxanthine-guanine phosphoribosyltransferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1919", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1919", 
            "name": "Hypoxanthine-guanine-phosphoribosyltransferase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1919", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:1919", 
        "name": "Lesch-Nyhan syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/1919#disease-associations", 
            "id": "1919", 
            "database": "Alliance of Genome Resources"
        }
    ]
}