{
    "disease_id": "DOID:0050726", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "type I tyrosinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "fumarylacetoacetate hydrolase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "FAH deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "hepatorenal tyrosinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "fumarylacetoacetase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "tyrosinemia, type I; TYRSN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "tyrosinemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "tyrosinemia, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "tyrosinemia, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010161", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010161", 
            "name": "TYRSN1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050726", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050726", 
            "name": "hepatorenal tyrosinemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050726", 
        "description": "A tyrosinemia that has_material_basis_in deficiency of the enzyme fumarylacetoacetate hydrolase resulting in an increase in fumarylacetoacetate which inhibits previous steps in tyrosine degradation leading to an accumulation of tyrosine in the body.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050726", 
        "name": "tyrosinemia type I"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050726#disease-associations", 
            "id": "0050726", 
            "database": "Alliance of Genome Resources"
        }
    ]
}