{
    "disease_id": "DOID:2352", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:2352", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2352", 
            "name": "diabetes bronze"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2352", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2352", 
            "name": "iron storage disorder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2352", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2352", 
            "name": "Haemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "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", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "neonatal hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "Nh"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "giant cell Hepatitis (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "Nhc"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "hemochromatosis, neonatal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "alloimmune Hepatitis, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "giant cell Hepatitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "giant cell Hepatitis, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "hemochromatosis neonatal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "neonatal Hepatitis, formerly"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "idiopathic neonatal hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "neonatal hepatitis (formerly)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009275", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009275", 
            "name": "neonatal Hepatitis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "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", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "hemochromatosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "HFE-associated hereditary hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "symptomatic form of hemochromatosis type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "HFE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "hemochromatosis, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "symptomatic form of HFE-related hereditary hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "symptomatic form of classic hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "HFE-related hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "hemochromatosis, type 1; HFE1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "classic hemochromatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0021001", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0021001", 
            "name": "C282Y/C282Y hemochromatosis"
        }, 
        {
            "url": "https://www.omim.org/entry/235200", 
            "description": "Hemochromatosis 1", 
            "resource": "MIM", 
            "id": "MIM:235200", 
            "name": "Hemochromatosis 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2352", 
        "description": "A metal metabolism disorder characterized by the accumulation of iron in various organs of the body.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2352", 
        "name": "hemochromatosis"
    }
}