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