{
    "disease_id": "DOID:2977", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "primary hyperoxaluria type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "hepatic AGT deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "hyperoxaluria, primary, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "peroxisomal alanine:glyoxylate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "glycolic aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "serine pyruvate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "hyperoxaluria, primary, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "alanine-glyoxylate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "peroxisomal alanine-glyoxylate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "hyperoxaluria, primary, type I; HP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "AGXT primary hyperoxaluria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "Oxalosis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "HP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "primary hyperoxaluria type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "peroxisomal alanine glyoxylate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "serine:pyruvate aminotransferase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009823", 
            "name": "primary hyperoxaluria caused by mutation in AGXT"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2977", 
        "description": "A carbohydrate metabolic disorder characterized by impaired glyoxylate metabolism resulting in accumulation of oxalate throughout the body typically manifesting as kidney and bladder stones.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2977", 
        "name": "primary hyperoxaluria"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2977#disease-associations", 
            "id": "2977", 
            "database": "Alliance of Genome Resources"
        }
    ]
}