{
    "disease_id": "DOID:3803", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "Crigler-Najjar syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "bilirubin-UGT deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "hyperbilirubinemia, Crigler-Najjar type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "UGT deficiency type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "hereditary unconjugated hyperbilirubinemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "Crigler-Najjar syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "Crigler Najjar syndrome, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021020", 
            "name": "Crigler-Najjar syndrome, type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3803", 
            "name": "Bilirubin UDP glucuronyl transferase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3803", 
            "name": "Crigler Najjar syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:3803", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:3803", 
            "name": "Crigler-Najjar syndrome, type I"
        }, 
        {
            "url": "https://www.omim.org/entry/218800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:218800", 
            "name": "Crigler-Najjar syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:3803", 
        "description": "A bilirubin metabolic disorder that involves a build up of bilirubin as bilirubin is not being broken down as a result of a lack or deficiency of the enzyme uridine diphosphate glycosyltransferase (UGT).", 
        "resource": "Disease Ontology", 
        "id": "DOID:3803", 
        "name": "Crigler-Najjar syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/218800", 
            "id": "218800", 
            "database": "MIM"
        }
    ]
}