{
    "disease_id": "DOID:1388",
    "recommended_name": {
        "id": "DOID:1388",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1388",
        "name": "Tangier disease",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:1388",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1388",
            "name": "familial alpha-lipoprotein deficiency",
            "description": ""
        },
        {
            "id": "DOID:1388",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1388",
            "name": "familial high density lipoprotein deficiency",
            "description": ""
        },
        {
            "id": "DOID:1388",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1388",
            "name": "familial hypoalphalipoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Tangier disease",
            "description": "Tangier disease (TD) is a rare lipoprotein metabolism disorder characterized biochemically by an almost complete absence of plasma high-density lipoproteins (HDL), and clinically by liver, spleen, lymph node and tonsil enlargement along with peripheral neuropathy in children and adolescents, and, occasionally, cardiovascular disease in adults."
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "HDL lipoprotein deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Analphalipoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Tangier disease; tgd",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "defective adenosine triphosphate-binding cassette transporter A1",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "familial hypoalphalipoproteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "cholesterol thesaurismosis",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "tgd",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Tangier disease",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "A-alphalipoprotein neuropathy",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Analphalipo-proteinemia",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "familial high density lipoprotein deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "high density lipoprotein deficiency, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "Alpha high density lipoprotein deficiency disease",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "HDLDT1",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "high density lipoprotein deficiency, Tangier type",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "ATP-binding cassette transporter A1 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "familial high density lipoprotein deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "familial alpha-lipoprotein deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0008783",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008783",
            "name": "familial Hypoalphalipo-proteinemia",
            "description": ""
        },
        {
            "id": "MIM:205400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/205400",
            "name": "Tangier disease",
            "description": "Tangier disease"
        }
    ]
}