{
    "disease_id": "DOID:0080957",
    "recommended_name": {
        "id": "DOID:0080957",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0080957",
        "name": "primary hypoalphalipoproteinemia 1",
        "description": "A hypolipoproteinemia that is characterized by low levels of high-density lipoprotein in the blood and that has_material_basis_in heterozygous mutation in the ABC1 gene on chromosome 9q31, which is also the site of mutations causing Tangier disease."
    },
    "synonyms": [
        {
            "id": "DOID:0080957",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080957",
            "name": "familial hypoalphalipoproteinemia",
            "description": ""
        },
        {
            "id": "DOID:0080957",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0080957",
            "name": "familial HDL deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "hypoalphalipoproteinemia, primary, 1",
            "description": "Any ypoalphalipoproteinemia in which the cause of the disease is a mutation in the ABCA1 gene."
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "HDL deficiency, familial, 1",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "hypoalphalipoproteinemia, familial",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "FHA",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "FHD",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "HDLD",
            "description": ""
        },
        {
            "id": "MONDO:0011393",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011393",
            "name": "familial HDL deficiency",
            "description": ""
        },
        {
            "id": "MIM:604091",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604091",
            "name": "Hypoalphalipoproteinemia, primary, 1",
            "description": "Hypoalphalipoproteinemia, primary, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0080957"
    ],
    "unlinked_id_list": []
}