{
    "disease_id": "DOID:0111672", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "HP3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "HOGA1 primary hyperoxaluria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "primary hyperoxaluria type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "PH III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "primary hyperoxaluria caused by mutation in HOGA1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "hyperoxaluria, primary, type III"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "hyperoxaluria, primary, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013327", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013327", 
            "name": "hyperoxaluria, primary, type III; HP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111672", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111672", 
            "name": "HP3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111672", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111672", 
            "name": "PH III"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111672", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111672", 
            "name": "primary hyperoxaluria type III"
        }, 
        {
            "url": "https://www.omim.org/entry/613616", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:613616", 
            "name": "Hyperoxaluria primary 3"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111672", 
        "description": "A primary hyperoxaluria characterized by recurring calcium oxalate stones that has_material_basis_in homozygous or compound heterozygous mutation in HOGA1 on chromosome 10q24.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111672", 
        "name": "primary hyperoxaluria type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/613616", 
            "id": "613616", 
            "database": "MIM"
        }
    ]
}