{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia, familial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "familial hypobetalipoproteinemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia, familial, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "APOB hypobetalipoproteinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia, familial, 1; FHBL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia, familial, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "acanthocytosis with hypobetalipoproteinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia caused by mutation in APOB"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "hypobetalipoproteinemia, Normotriglyceridemic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "FHBL1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014252", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014252", 
            "name": "FHBL"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111062", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111062", 
            "name": "FHBL1"
        }, 
        {
            "url": "https://www.omim.org/entry/615558", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:615558", 
            "name": "Hypobetalipoproteinemia, familial, 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111062", 
        "description": "A hypobetalipoproteinemia that has material_basis_in mutation in the APOB gene on chromosome 2p24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111062", 
        "name": "familial hypobetalipoproteinemia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/615558", 
            "id": "615558", 
            "database": "MIM"
        }
    ]
}