{
    "disease_id": "DOID:0111136", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "congenital generalized lipodystrophy (disease) caused by mutation in BSCL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "lipoatrophic diabetes, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
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        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "congenital lipoatrophic diabetes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "BSCL2 congenital generalized lipodystrophy (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Berardinelli-Seip syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "CGL2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Seip syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "BSCL2-related Brunzell syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Berardinelli Seip congenital lipodystrophy type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Brunzell syndrome, BSCL2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Berardinelli syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "total lipodystrophy and acromegaloid gigantism"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "Brunzell syndrome BSCL2-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "lipodystrophy, Berardinelli-Seip congenital, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010020", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010020", 
            "name": "lipodystrophy, congenital generalized, type 2; CGL2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "Berardinelli-Seip congenital lipodystrophy type 2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "Berardinelli-Seip syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "Brunzell syndrome BSCL2-related"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "CGL2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "congenital lipoatrophic diabetes"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111136", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111136", 
            "name": "total lipodystrophy and acromegaloid gigantism"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111136", 
        "description": "A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of BSCL2 on chromosome 11q12.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111136", 
        "name": "congenital generalized lipodystrophy type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111136#disease-associations", 
            "id": "0111136", 
            "database": "Alliance of Genome Resources"
        }
    ]
}