{
    "disease_id": "DOID:0111370",
    "recommended_name": {
        "id": "DOID:0111370",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111370",
        "name": "apolipoprotein C-III deficiency",
        "description": "A cholesterol-ester transfer protein deficiency characterized by elevated levels of alpha-lipoprotein in the blood that has_material_basis_in heterozygous mutation in the APOC3 gene on chromosome 11q23.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111370",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111370",
            "name": "HALP2",
            "description": ""
        },
        {
            "id": "DOID:0111370",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111370",
            "name": "hyperalphalipoproteinemia 2",
            "description": ""
        },
        {
            "id": "MONDO:0013534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013534",
            "name": "apolipoprotein c-III deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013534",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013534",
            "name": "apolipoprotein c-III deficiency",
            "description": ""
        },
        {
            "id": "MIM:614028",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614028",
            "name": "Hyperalphalipoproteinemia 2",
            "description": "Hyperalphalipoproteinemia 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111370"
    ],
    "unlinked_id_list": []
}