{
    "disease_id": "DOID:9245", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Alagille syndrome due to a NOTCH2 point mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Alagille syndrome 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Alagille syndrome type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Alagille syndrome 2; ALGS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Alagille-Watson syndrome due to a NOTCH2 point mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "ALGS2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "Arteriohepatic dysplasia due to a NOTCH2 point mutation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012439", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012439", 
            "name": "syndromic bile duct paucity due to a NOTCH2 point mutation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9245", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9245", 
            "name": "Alagille-Watson syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:9245", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:9245", 
            "name": "Arteriohepatic dysplasia"
        }, 
        {
            "url": "https://www.omim.org/entry/610205", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:610205", 
            "name": "Alagille syndrome 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:9245", 
        "description": "A liver disease that is characterized by an accumulation of bile in the liver resulting from a reducted number of liver small bile ducts.", 
        "resource": "Disease Ontology", 
        "id": "DOID:9245", 
        "name": "Alagille syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/610205", 
            "id": "610205", 
            "database": "MIM"
        }
    ]
}