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