{
    "disease_id": "DOID:0080479",
    "recommended_name": {
        "id": "DOID:0080479",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0080479",
        "name": "peroxisome biogenesis disorder 4A",
        "description": "A peroxisomal biogenesis disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PEX6 gene on chromosome 6p21.1."
    },
    "synonyms": [
        {
            "id": "DOID:0080479",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0080479",
            "name": "peroxisome biogenesis disorder 4A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder 4A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder 4A (Zellweger); PBD4A",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder 4A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder, complementation group 6",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "PBD4A",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder, complementation group 4",
            "description": ""
        },
        {
            "id": "MONDO:0013930",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013930",
            "name": "peroxisome biogenesis disorder, complementation group C",
            "description": ""
        },
        {
            "id": "MIM:614862",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614862",
            "name": "Peroxisome biogenesis disorder 4A",
            "description": "Peroxisome biogenesis disorder 4A"
        }
    ]
}