{
    "disease_id": "DOID:0080716", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "infantile liver failure syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "ILFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "infantile liver failure syndrome 1; ILFS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "infantile liver failure syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "LARS infantile liver failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "infantile liver failure caused by mutation in LARS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0024568", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0024568", 
            "name": "acute infantile liver failure - multisystemic involvement syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080716", 
        "description": "A syndrome that is characterized by acute liver failure, that occurs in the first year of life, which manifests with failure to thrive, hypotonia, moderate global developmental delay, seizures, abnormal liver function tests, microcytic anemia and elevated serum lactate.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080716", 
        "name": "infantile liver failure syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080716#disease-associations", 
            "id": "0080716", 
            "database": "Alliance of Genome Resources"
        }
    ]
}