{
    "disease_id": "DOID:14118", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipoproteinemia, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "lipoprotein lipase deficiency, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperchylomicronemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "mixed hyperglyceridemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial lipoprotein lipase deficiency (disorder) [ambiguous]"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "lipd deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperchylomicronemia, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipoproteinemia type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipoproteinemia, type 1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial fat-induced hypertriglyceridemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial hyperlipoproteinemia type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "lipase D deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "chylomicronemia, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipemia, idiopathic, Burger-Grutz type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "endogenous hypertriglyceridaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipoproteinemia, type I"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "LPL deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "Burger-Grutz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "lipoprotein lipase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial lipoprotein lipase deficiency with type I phenotype"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "type I hyperlipoproteinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "Fredrickson type I lipaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial LPL deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial hyperchylomicronemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hyperlipemia, essential familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "familial chylomiconemia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "hypercholesterinaemic xanthomatosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009387", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009387", 
            "name": "Fredrickson type I hyperlipoproteinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "Fredrickson type I hyperlipoproteinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "Fredrickson type I lipaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "familial LPL deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "familial chylomicronemia syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "familial hyperlipoproteinemia type I"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "hypercholesterinaemic xanthomatosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "hyperchylomicronemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14118", 
            "name": "mixed hyperglyceridemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14118", 
        "description": "A familial hyperlipemia characterized by a deficiency of the enzyme lipoprotein lipase and the subsequent build up of chylomicrons and increased plasma concentration of triglycerides.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14118", 
        "name": "familial lipoprotein lipase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14118#disease-associations", 
            "id": "14118", 
            "database": "Alliance of Genome Resources"
        }
    ]
}