{
    "disease_id": "DOID:0111370", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013534", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013534", 
            "name": "hyperalphalipoproteinemia 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111370", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111370", 
            "name": "HALP2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111370", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111370", 
            "name": "hyperalphalipoproteinemia 2"
        }, 
        {
            "url": "https://www.omim.org/entry/614028", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:614028", 
            "name": "Hyperalphalipoproteinemia 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111370", 
        "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 APOC3 on chromosome 11q23.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111370", 
        "name": "apolipoprotein C-III deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/614028", 
            "id": "614028", 
            "database": "MIM"
        }
    ]
}