{
    "disease_id": "DOID:0080622", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008736", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008736", 
            "name": "peroxisome biogenesis disorder type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008736", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008736", 
            "name": "peroxisome biogenesis disorder 2B; PBD2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008736", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008736", 
            "name": "PBD2B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080622", 
        "description": "A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX5 gene on chromosome 12p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080622", 
        "name": "peroxisome biogenesis disorder 2B"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/202370", 
            "id": "202370", 
            "database": "MIM"
        }
    ]
}