{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "peroxisome biogenesis disorder 12A (Zellweger)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "peroxisome biogenesis disorder, complementation group 14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "peroxisome biogenesis disorder 12A (Zellweger); PBD12A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "peroxisome biogenesis disorder, complementation group J"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "PBD12A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "Cg14"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013951", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013951", 
            "name": "Cgj"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080486", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080486", 
            "name": "peroxisome biogenesis disorder 12A (Zellweger)"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080486", 
        "description": "A peroxisomal biogenesis disorder that has_material_basis_in homozygous mutation in the PEX19 gene on chromosome 1q23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080486", 
        "name": "peroxisome biogenesis disorder 12A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614886", 
            "id": "614886", 
            "database": "MIM"
        }
    ]
}