{
    "disease_id": "DOID:0111029",
    "recommended_name": {
        "id": "DOID:0111029",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111029",
        "name": "hemochromatosis type 1",
        "description": "A hemochromatosis that has_material_basis_in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22."
    },
    "synonyms": [
        {
            "id": "DOID:0111029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111029",
            "name": "HFE1",
            "description": ""
        },
        {
            "id": "DOID:0111029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111029",
            "name": "symptomatic form of classic hemochromatosis",
            "description": ""
        },
        {
            "id": "DOID:0111029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111029",
            "name": "symptomatic form of hemochromatosis type 1",
            "description": ""
        },
        {
            "id": "DOID:0111029",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111029",
            "name": "symptomatic form of HFE-related hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "hemochromatosis type 1",
            "description": "Hemochromatosis type 1 (classic) is the most common form of hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition. Due to its incidence (1/200-1/1000), it is not considered as a rare disease, unlike the other subforms of the disease"
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "C282Y/C282Y hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "HFE-associated hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "HFE-related hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "HFE1",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "classic hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "hemochromatosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "hemochromatosis, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "hfe hemochromatosis, modifier of",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "symptomatic form of hemochromatosis type 1",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "symptomatic form of HFE-related hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "symptomatic form of classic hemochromatosis",
            "description": ""
        },
        {
            "id": "MIM:235200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/235200",
            "name": "Hemochromatosis 1",
            "description": "Hemochromatosis 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111029"
    ],
    "unlinked_id_list": []
}