{
    "disease_id": "DOID:0080487",
    "recommended_name": {
        "id": "DOID:0080487",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080487",
        "name": "peroxisome biogenesis disorder 13A",
        "description": "A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX14 gene on chromosome 1p36."
    },
    "synonyms": [
        {
            "id": "DOID:0080487",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080487",
            "name": "peroxisome biogenesis disorder 13A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013952",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013952",
            "name": "peroxisome biogenesis disorder 13A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013952",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013952",
            "name": "peroxisome biogenesis disorder 13A (Zellweger)",
            "description": ""
        },
        {
            "id": "MONDO:0013952",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013952",
            "name": "PBD13A",
            "description": ""
        },
        {
            "id": "MIM:614887",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614887",
            "name": "Peroxisome biogenesis disorder complementation group K",
            "description": "Peroxisome biogenesis disorder complementation group K"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080487"
    ],
    "unlinked_id_list": []
}