{
    "disease_id": "DOID:0111369",
    "recommended_name": {
        "id": "DOID:0111369",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111369",
        "name": "hyperalphalipoproteinemia 1",
        "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 CETP gene on chromosome 16q13."
    },
    "synonyms": [
        {
            "id": "DOID:0111369",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111369",
            "name": "HALP1",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "cholesterol-ester transfer protein deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "hyperalphalipoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "CEPT deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "familial hyperalphalipoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "high density lipoprotein cholesterol level QTL 10",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "hyperalphalipoproteinemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "hyperalphalipoproteinemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "CETP deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "HALP1",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "Hdlcq10",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "cholesterol ester transfer Protein deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0007744",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007744",
            "name": "high density lipoprotein cholesterol level quantitative trait locus 10",
            "description": ""
        },
        {
            "id": "MIM:143470",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/143470",
            "name": "Hyperalphalipoproteinemia 1",
            "description": "Hyperalphalipoproteinemia 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111369"
    ],
    "unlinked_id_list": []
}