{
    "disease_id": "DOID:0111418",
    "recommended_name": {
        "id": "DOID:0111418",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111418",
        "name": "familial apolipoprotein C-II deficiency",
        "description": "A familial chylomicronemia syndrome characterized by onset in adolescence or adulthood of hypertriglyceridemia and fasting chylomicronemia that has_material_basis_in homozygous or compound heterozygous mutation in the APOC2 gene on chromosome 19q13.32."
    },
    "synonyms": [
        {
            "id": "DOID:0111418",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111418",
            "name": "C-II anapolipoproteinemia",
            "description": ""
        },
        {
            "id": "DOID:0111418",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111418",
            "name": "familial APOC2 deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111418",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111418",
            "name": "familial apoC-II deficiency",
            "description": ""
        },
        {
            "id": "DOID:0111418",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111418",
            "name": "hyperlipoproteinemia, type 1b",
            "description": ""
        },
        {
            "id": "DOID:0111418",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111418",
            "name": "hyperlipoproteinemia, type Ib",
            "description": ""
        },
        {
            "id": "MONDO:0008810",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008810",
            "name": "familial apolipoprotein C-II deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008810",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008810",
            "name": "familial apoC-II deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008810",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008810",
            "name": "familial apolipoprotein C-II deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008810",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008810",
            "name": "hyperlipoproteinemia, type IB",
            "description": ""
        },
        {
            "id": "MIM:207750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/207750",
            "name": "Hyperlipoproteinemia 1B",
            "description": "Hyperlipoproteinemia 1B"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111418"
    ],
    "unlinked_id_list": []
}