{
    "disease_id": "DOID:0070221", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "progressive familial intrahepatic cholestasis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "cholestasis, progressive familial intrahepatic, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "severe ATP8B1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "cholestasis, fatal intrahepatic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "Byler disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "PFIC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "cholestasis, progressive familial intrahepatic, 1; PFIC1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "FIC1 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "Byler's disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008892", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008892", 
            "name": "cholestasis, progressive familial intrahepatic, type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070221", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070221", 
            "name": "PFIC; Byler disease"
        }, 
        {
            "url": "https://www.omim.org/entry/211600", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:211600", 
            "name": "Cholestasis, progressive familial intrahepatic, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070221", 
        "description": "An intrahepatic cholestasis characterized by early onset of chronic unremitting cholestasis of hepatocellular origin that progresses to hepatic fibrosis, cirrhosis, and end-stage liver disease before adulthood.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070221", 
        "name": "progressive familial intrahepatic cholestasis"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/211600", 
            "id": "211600", 
            "database": "MIM"
        }
    ]
}