{
    "disease_id": "DOID:0080778", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "acute infantile liver failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "LFIT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "infantile liver failure caused by mutation in TRMU"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "liver failure, infantile, transient"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "liver failure, infantile, transient; LFIT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013111", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013111", 
            "name": "TRMU infantile liver failure"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080778", 
        "description": "A liver disease that is characterized by elevated liver enzymes, jaundice, vomiting, coagulopathy, and hyperbilirubinemia, and the presence of increased serum lactate and that has_material_basis_in homozygous or compound heterozygous mutation in the TRMU gene, which is involved in mitochondrial protein translation, on chromosome 22q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080778", 
        "name": "transient infantile liver failure"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080778#disease-associations", 
            "id": "0080778", 
            "database": "Alliance of Genome Resources"
        }
    ]
}