{
    "disease_id": "DOID:0050727",
    "recommended_name": {
        "id": "DOID:0050727",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050727",
        "name": "tyrosinemia type III",
        "description": "A tyrosinemia that has_material_basis_in deficiency of 4-hydroxyphenylpyruvate dioxygenase disrupting the break down of tyrosine."
    },
    "synonyms": [
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia type III",
            "description": "Tyrosinemia type 3 is an inborn error of tyrosine metabolism characterized by mild hypertyrosinemia and increased urinary excretion of 4-hydroxyphenylpyruvate, 4-hydroxyphenyllactate and 4-hydroxyphenylacetate."
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia due to HPD deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia type III",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "4-alpha hydroxyphenylpyruvate dioxygenase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "4-alpha hydroxyphenylpyruvic acid oxidase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "TYRSN3",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia type 3",
            "description": ""
        },
        {
            "id": "MONDO:0010162",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010162",
            "name": "tyrosinemia, type III",
            "description": ""
        },
        {
            "id": "MIM:276710",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/276710",
            "name": "Tyrosinemia 3",
            "description": "Tyrosinemia 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050727"
    ],
    "unlinked_id_list": []
}