{
    "disease_id": "DOID:2352",
    "recommended_name": {
        "id": "DOID:2352",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:2352",
        "name": "hemochromatosis",
        "description": "A metal metabolism disorder characterized by the accumulation of iron in various organs of the body."
    },
    "synonyms": [
        {
            "id": "DOID:2352",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2352",
            "name": "Haemochromatosis",
            "description": ""
        },
        {
            "id": "DOID:2352",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2352",
            "name": "diabetes bronze",
            "description": ""
        },
        {
            "id": "DOID:2352",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:2352",
            "name": "iron storage disorder",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "neonatal hemochromatosis",
            "description": "Neonatal hemochromatosis is a disease in which too much iron builds up inthe body. In this form of hemochromatosis the iron overload begins before birth. This disease tends to progress rapidly and is characterized by liver damage that is apparent at birth or in the first day of life. There are a number of other forms of hemochromatosis. To learn more about these other forms click on the disease names listed below: Hemochromatosis type 1 Hemochromatosis type 2 Hemochromatosis type 3 Hemochromatosis type 4"
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "giant cell Hepatitis",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "neonatal hepatitis (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "hemochromatosis, neonatal",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "alloimmune Hepatitis, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "idiopathic neonatal hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "neonatal Hepatitis, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "neonatal Hepatitis",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "giant cell Hepatitis (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "Nh",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "giant cell Hepatitis, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "hemochromatosis neonatal",
            "description": ""
        },
        {
            "id": "MONDO:0009275",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009275",
            "name": "Nhc",
            "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": "hemochromatosis, type 1",
            "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": "HFE-related hemochromatosis",
            "description": ""
        },
        {
            "id": "MONDO:0021001",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0021001",
            "name": "symptomatic form of classic hemochromatosis",
            "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": "hemochromatosis, type 1; 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": "C282Y/C282Y hemochromatosis",
            "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": "HFE-associated hereditary hemochromatosis",
            "description": ""
        },
        {
            "id": "MIM:235200",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/235200",
            "name": "Hemochromatosis 1",
            "description": "Hemochromatosis 1"
        }
    ]
}