{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthinuria type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "XO deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthinuria type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "XOR deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthine oxidoreductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthinuria, type I; XAN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthinuria, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "hereditary xanthinuria, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthine oxidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "XDH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthine dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "isolated xanthine oxidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "type 1 xanthinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "XAN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010209", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010209", 
            "name": "xanthinuria, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060236", 
            "name": "xanthine dehydrogenase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060236", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060236", 
            "name": "xanthine oxidase deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/278300", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:278300", 
            "name": "Xanthinuria 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060236", 
        "description": "A purine-pyrimidine metabolic disorder characterized by deficiency of xanthine oxidase, resulting in excretion of large amounts of xanthine in the urine and the formation of xanthine stones.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060236", 
        "name": "xanthinuria"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/278300", 
            "id": "278300", 
            "database": "MIM"
        }
    ]
}