{
    "disease_id": "DOID:0111418", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "hyperlipoproteinemia, type IB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "Apoc2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "C-II Anapolipoproteinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "hyperlipoproteinemia, type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "apolipoprotein C-II deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008810", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008810", 
            "name": "familial apoC-II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111418", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111418", 
            "name": "C-II anapolipoproteinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111418", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111418", 
            "name": "familial APOC2 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111418", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111418", 
            "name": "familial apoC-II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111418", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111418", 
            "name": "hyperlipoproteinemia, type 1b"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111418", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111418", 
            "name": "hyperlipoproteinemia, type Ib"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111418", 
        "description": "A familial chylomicronemia syndrome characterized by onset in adolescence or adulthood of hypertriglyceridemia and fasting chylomicronemia that has_material_basis_in homozygous or compound heterozygous mutation in APOC2 on chromosome 19q13.32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111418", 
        "name": "familial apolipoprotein C-II deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111418#disease-associations", 
            "id": "0111418", 
            "database": "Alliance of Genome Resources"
        }
    ]
}