{
    "disease_id": "DOID:0111420", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014412", 
            "name": "hyperlipoproteinemia, type 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014412", 
            "name": "GPIHBP1 familial hyperlipidemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014412", 
            "name": "familial hyperlipidemia caused by mutation in GPIHBP1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014412", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014412", 
            "name": "hyperlipoproteinemia, type ID"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111420", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111420", 
            "name": "familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111420", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111420", 
            "name": "hyperlipoproteinemia type 1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111420", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111420", 
            "name": "hyperlipoproteinemia type ID"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111420", 
        "description": "A familial chylomicronemia syndrome characterized by refactory fasting hyperchylomicronemia, and elevated plasma triglyceride levels that has_material_basis_in homozygous or compound heterozygous mutation in GPIHBP1 on chromosome 8q24.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111420", 
        "name": "familial GPIHBP1 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111420#disease-associations", 
            "id": "0111420", 
            "database": "Alliance of Genome Resources"
        }
    ]
}