{
    "disease_id": "DOID:0111061", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "hypobetalipoproteinemia, familial, 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "hypobetalipoproteinemia, familial, 2; FHBL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "FHBL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "combined familial hypolipidemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "hypobetalipoproteinemia caused by mutation in ANGPTL3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "hypolipidemia, familial, combined"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "familial hypobetalipoproteinemia type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "hypobetalipoproteinemia, familial, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011505", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011505", 
            "name": "ANGPTL3 hypobetalipoproteinemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111061", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111061", 
            "name": "FHBL2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111061", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111061", 
            "name": "combined familial hypolipidemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111061", 
        "description": "A hypobetalipoproteinemia that has material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111061", 
        "name": "familial hypobetalipoproteinemia 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111061#disease-associations", 
            "id": "0111061", 
            "database": "Alliance of Genome Resources"
        }
    ]
}