{
    "disease_id": "DOID:0111672",
    "recommended_name": {
        "id": "DOID:0111672",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111672",
        "name": "primary hyperoxaluria type 3",
        "description": "A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in the HOGA1 gene on chromosome 10q24.2."
    },
    "synonyms": [
        {
            "id": "DOID:0111672",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111672",
            "name": "HP3",
            "description": ""
        },
        {
            "id": "DOID:0111672",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111672",
            "name": "PH III",
            "description": ""
        },
        {
            "id": "DOID:0111672",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111672",
            "name": "primary hyperoxaluria type III",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "primary hyperoxaluria type 3",
            "description": "Primary hyperoxaluria type 3 (PH3) is a disorder of glyoxylate metabolism that can be asymptomatic or characterized by oxalate nephrolithiasis."
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "HOGA1 primary hyperoxaluria",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "primary hyperoxaluria caused by mutation in HOGA1",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "primary hyperoxaluria type III",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "HP3",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "PH III",
            "description": ""
        },
        {
            "id": "MONDO:0013327",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013327",
            "name": "hyperoxaluria, primary, type III",
            "description": ""
        },
        {
            "id": "MIM:613616",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613616",
            "name": "Hyperoxaluria primary 3",
            "description": "Hyperoxaluria primary 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111672"
    ],
    "unlinked_id_list": []
}