{
    "disease_id": "DOID:0080485", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013949", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013949", 
            "name": "peroxisome biogenesis disorder 11A (Zellweger)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013949", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013949", 
            "name": "peroxisome biogenesis disorder 11A (Zellweger); PBD11A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013949", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013949", 
            "name": "peroxisome biogenesis disorder, complementation group 13"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013949", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013949", 
            "name": "peroxisome biogenesis disorder, complementation group H"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013949", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013949", 
            "name": "PBD11A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080485", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080485", 
            "name": "peroxisome biogenesis disorder 11A (Zellweger)"
        }, 
        {
            "url": "https://www.omim.org/entry/614883", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614883", 
            "name": "Peroxisome biogenesis disorder complementation group 13"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080485", 
        "description": "A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080485", 
        "name": "peroxisome biogenesis disorder 11A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614883", 
            "id": "614883", 
            "database": "MIM"
        }
    ]
}