{
    "disease_id": "DOID:0111422", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "lipase deficiency, combined"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "lipase deficiency combined"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "combined lipase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "LPL and HTGL deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009527", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009527", 
            "name": "LPL and HL deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111422", 
            "name": "LPL and HL deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111422", 
            "name": "LPL and HTGL deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111422", 
            "name": "combined lipase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111422", 
            "name": "familial LMF1 deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111422", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111422", 
            "name": "lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111422", 
        "description": "A familial chylomicronemia syndrome characterized by hypertriglyceridemia, chylomicronemia, and decreased lipase activity that has_material_basis_in homozygous mutation in LMF1 on chromosome 16p13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111422", 
        "name": "familial lipase maturation factor 1 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111422#disease-associations", 
            "id": "0111422", 
            "database": "Alliance of Genome Resources"
        }
    ]
}