{
    "disease_id": "DOID:0080478", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013927", 
            "name": "peroxisome biogenesis disorder 3A (Zellweger)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013927", 
            "name": "peroxisome biogenesis disorder 3A (Zellweger); PBD3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013927", 
            "name": "PBD3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013927", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013927", 
            "name": "peroxisome biogenesis disorder, complementation group 3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080478", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080478", 
            "name": "peroxisome biogenesis disorder 3A (Zellweger)"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080478", 
        "description": "A peroxisomal biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX12 gene on chromosome 17.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080478", 
        "name": "peroxisome biogenesis disorder 3A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614859", 
            "id": "614859", 
            "database": "MIM"
        }
    ]
}