{
    "disease_id": "DOID:0050763", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "arthrogryposis, renal dysfunction, and cholestasis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "arthrogryposis, renal dysfunction, and cholestasis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VPS33B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "VPS33B arthrogryposis-renal dysfunction-cholestasis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "arthrogryposis, renal dysfunction, and cholestasis 1; ARCS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008822", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008822", 
            "name": "ARCS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050763", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050763", 
            "name": "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050763", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050763", 
            "name": "Arthrogryposis-renal dysfunction-cholestasis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050763", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050763", 
            "name": "Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/208085", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:208085", 
            "name": "Arthrogryposis, renal dysfunction and cholestasis syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050763", 
        "description": "A syndrome that is characterized by congenital joint contractures, renal tubular dysfunction, cholestasis, severe failure to thrive, ichthyosis and a defect in platelet alpha-granule biogenesis and that has_material_basis_in homozygous or compound heterozygous mutation in the VPS33B gene or homozygous or compound heterozygous mutation in the VIPAR gene on chromosome 14q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050763", 
        "name": "ARC syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/208085", 
            "id": "208085", 
            "database": "MIM"
        }
    ]
}