{
    "disease_id": "DOID:0111032",
    "recommended_name": {
        "id": "DOID:0111032",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111032",
        "name": "hemochromatosis type 2B",
        "description": "A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111032",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111032",
            "name": "HFE2B",
            "description": ""
        },
        {
            "id": "MONDO:0013220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013220",
            "name": "hemochromatosis type 2B",
            "description": "Any hemochromatosis type 2 in which the cause of the disease is a mutation in the HAMP gene."
        },
        {
            "id": "MONDO:0013220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013220",
            "name": "HAMP hemochromatosis type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013220",
            "name": "HFE2B",
            "description": ""
        },
        {
            "id": "MONDO:0013220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013220",
            "name": "hemochromatosis type 2 caused by mutation in HAMP",
            "description": ""
        },
        {
            "id": "MONDO:0013220",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013220",
            "name": "hemochromatosis, type 2B",
            "description": ""
        },
        {
            "id": "MIM:613313",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613313",
            "name": "Hemochromatosis 2B",
            "description": "Hemochromatosis 2B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111032"
    ],
    "unlinked_id_list": []
}