{
    "disease_id": "DOID:0111030",
    "recommended_name": {
        "id": "DOID:0111030",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111030",
        "name": "hemochromatosis type 3",
        "description": "A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the TFR2 gene on chromosome 7q22."
    },
    "synonyms": [
        {
            "id": "DOID:0111030",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111030",
            "name": "HFE3",
            "description": ""
        },
        {
            "id": "DOID:0111030",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111030",
            "name": "TFR2-related hemochromatosis",
            "description": ""
        },
        {
            "id": "DOID:0111030",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111030",
            "name": "hemochromatosis due to defect in transferrin receptor 2",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "hemochromatosis type 3",
            "description": "Type 3 hemochromatosis is a form of rare hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition of genetic origin."
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "HFE3",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "TFR2 hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "TFR2-related hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "hemochromatosis type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "hereditary hemochromatosis caused by mutation in TFR2",
            "description": ""
        },
        {
            "id": "MONDO:0011417",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011417",
            "name": "hemochromatosis, type 3",
            "description": ""
        },
        {
            "id": "MIM:604250",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604250",
            "name": "Hemochromatosis 3",
            "description": "Hemochromatosis 3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111030"
    ],
    "unlinked_id_list": []
}