{
    "disease_id": "DOID:0050464", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "Farber's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "N-Laurylsphingosine deacylase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "FRBRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "Farber lipogranulomatosis; FRBRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "AC deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "Farber disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "acid ceramidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009218", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009218", 
            "name": "ceramidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050464", 
            "name": "Farber disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050464", 
            "name": "N-laurylsphingosine deacylase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050464", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050464", 
            "name": "acid ceramidase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050464", 
        "description": "A lipid storage disease that is characterized by abnormalities in swallowing, cognition, joint function, and central nervous system due to a deficiency in the enzyme ceramidase that results in sphingolipids deposition.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050464", 
        "name": "Farber lipogranulomatosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050464#disease-associations", 
            "id": "0050464", 
            "database": "Alliance of Genome Resources"
        }
    ]
}