{
    "disease_id": "DOID:0111136",
    "recommended_name": {
        "id": "DOID:0111136",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111136",
        "name": "congenital generalized lipodystrophy type 2",
        "description": "A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of BSCL2 on chromosome 11q12.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "Berardinelli-Seip congenital lipodystrophy type 2",
            "description": ""
        },
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "Berardinelli-Seip syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "Brunzell syndrome BSCL2-related",
            "description": ""
        },
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "CGL2",
            "description": ""
        },
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "congenital lipoatrophic diabetes",
            "description": ""
        },
        {
            "id": "DOID:0111136",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111136",
            "name": "total lipodystrophy and acromegaloid gigantism",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "congenital generalized lipodystrophy type 2",
            "description": "Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the BSCL2 gene."
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "BSCL2 congenital generalised lipodystrophy (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "BSCL2 congenital generalized lipodystrophy (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Berardinelli-Seip congenital lipodystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Berardinelli-Seip syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Brunzell syndrome BSCL2-related",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "CGL2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "congenital generalised lipodystrophy (disease) caused by mutation in BSCL2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "congenital generalized lipodystrophy (disease) caused by mutation in BSCL2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "congenital lipoatrophic diabetes",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "total lipodystrophy and acromegaloid gigantism",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "BSCL2-related Brunzell syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Berardinelli Seip congenital lipodystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Berardinelli syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Berardinelli-Seip congenital lipodystrophy, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Brunzell syndrome, BSCL2-related",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "Seip syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "lipoatrophic diabetes, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "lipodystrophy, Berardinelli-Seip congenital, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "lipodystrophy, congenital generalized, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010020",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010020",
            "name": "lipodystrophy, total, and acromegaloid gigantism",
            "description": ""
        },
        {
            "id": "MIM:269700",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/269700",
            "name": "Congenital generalized lipodystrophy 2",
            "description": "Congenital generalized lipodystrophy 2"
        }
    ]
}