{
    "disease_id": "DOID:0060350", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "nephrolithiasis, Dha"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "Dihydroxyadeninuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "urolithiasis, 2,8-dihydroxyadenine"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "APRTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "2,8-dihydroxyadenine urolithiasis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "adenine phosphoribosyltransferase deficiency; APRTD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "APRT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "urolithiasis, Dha"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013869", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013869", 
            "name": "2,8-dihydroxyadeninuria disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060350", 
            "name": "2,8-dihydroxyadenine urolithiasis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060350", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060350", 
            "name": "APRT deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060350", 
        "description": "An amino acid metabolic disorder characterized by the formation 2,8-dihydroxyadenine stones and renal failure secondary to intratubular crystalline precipitation. It has an autosomal recessive inheritance pattern.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060350", 
        "name": "adenine phosphoribosyltransferase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060350#disease-associations", 
            "id": "0060350", 
            "database": "Alliance of Genome Resources"
        }
    ]
}