{
    "disease_id": "DOID:0111135",
    "recommended_name": {
        "id": "DOID:0111135",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111135",
        "name": "congenital generalized lipodystrophy type 1",
        "description": "A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3."
    },
    "synonyms": [
        {
            "id": "DOID:0111135",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111135",
            "name": "Berardinelli-Seip Congenital Lipodystrophy, Type 1",
            "description": ""
        },
        {
            "id": "DOID:0111135",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111135",
            "name": "Brunzell syndrome AGPAT2-related",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "congenital generalized lipodystrophy type 1",
            "description": "Any congenital generalized lipodystrophy in which the cause of the disease is a mutation in the AGPAT2 gene."
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "AGPAT2 congenital generalised lipodystrophy (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "AGPAT2 congenital generalized lipodystrophy (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "BSCL1",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "Berardinelli-Seip congenital lipodystrophy, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "CGL1",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "congenital generalised lipodystrophy (disease) caused by mutation in AGPAT2",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "congenital generalized lipodystrophy (disease) caused by mutation in AGPAT2",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "congenital generalized lipodystrophy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "AGPAT2-related Brunzell syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "Berardinelli-Seip congenital lipodystrophy type 1",
            "description": ""
        },
        {
            "id": "MONDO:0012071",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012071",
            "name": "lipodystrophy, congenital generalized, type 1",
            "description": ""
        },
        {
            "id": "MIM:608594",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608594",
            "name": "Lipodystrophy, congenital generalized, 1",
            "description": "Lipodystrophy, congenital generalized, 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111135"
    ],
    "unlinked_id_list": []
}