{
    "disease_id": "DOID:0111671", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "GRHPR primary hyperoxaluria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "glyoxylate reductase/hydroxypyruvate reductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "primary hyperoxaluria caused by mutation in GRHPR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "glyceric aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "hyperoxaluria, primary, type II; HP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "hyperoxaluria, primary, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "D-glycerate dehydrogenase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "Oxalosis 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "HP2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "L-glyceric aciduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "hyperoxaluria, primary, type II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009824", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009824", 
            "name": "primary hyperoxaluria type II"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111671", 
            "name": "oxalosis IIglyoxylate reductase/hydroxypyruvate reductase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111671", 
            "name": "D-glycerate dehydrogenase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111671", 
            "name": "HP2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111671", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111671", 
            "name": "L-glyceric aciduria"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111671", 
        "description": "A primary hyperoxaluria characterized by elevated urinary excretion of oxalate and L-glycerate, recurrent nephrolithiasis and nephrocalcinosis, and end-stage renal disease that has_material_basis_in homozygous or compound heterozygous mutation in GRHPR on chromosome 9p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111671", 
        "name": "primary hyperoxaluria type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111671#disease-associations", 
            "id": "0111671", 
            "database": "Alliance of Genome Resources"
        }
    ]
}