{
    "disease_id": "DOID:0080632", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008890", 
            "name": "progressive bulbar palsy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008890", 
            "name": "progressive bulbar atrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008890", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008890", 
            "name": "bulbar palsy, progressive, of childhood"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080632", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080632", 
            "name": "riboflavin transporter deficiency neuronopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080632", 
        "description": "A progressive bulbar palsy that is characterized by motor, sensory and cranial neuronopathy and that has_material_basis_in homozygous mutation in the C20ORF54 gene on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080632", 
        "name": "Fazio-Londe disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080632#disease-associations", 
            "id": "0080632", 
            "database": "Alliance of Genome Resources"
        }
    ]
}