{
    "disease_id": "DOID:0050797",
    "recommended_name": {
        "id": "DOID:0050797",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050797",
        "name": "peroxisomal acyl-CoA oxidase deficiency",
        "description": "A peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy."
    },
    "synonyms": [
        {
            "id": "DOID:0050797",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050797",
            "name": "Peroxisomal acyl-coenzyme A oxidase",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "peroxisomal acyl-CoA oxidase deficiency",
            "description": "Peroxisomal acyl-CoA oxidase deficiency is a rare neurodegenerative disorder that belongs to the group of inherited peroxisomal disorders and is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy."
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "ACOX1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "Pseudoadrenoleukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "peroxisomal acyl-CoA oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "peroxisomal acyl-coenzyme A oxidase",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "pseudo-NALD",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "pseudo-neonatal adrenoleukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "Pseudoneonatal adrenoleukodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0009919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009919",
            "name": "straight-chain acyl-Coa oxidase deficiency",
            "description": ""
        },
        {
            "id": "MIM:264470",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/264470",
            "name": "Adrenoleukodystrophy, pseudoneonatal",
            "description": "Adrenoleukodystrophy, pseudoneonatal"
        }
    ]
}