{
    "disease_id": "DOID:0050585",
    "recommended_name": {
        "id": "DOID:0050585",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050585",
        "name": "congenital generalized lipodystrophy",
        "description": "A lipodystrophy that is characterized by extreme scarcity of subcutaneous fat, muscular hypertrophy, fatty liver, hypertriglyceremia and metabolic complications including insulin resistance."
    },
    "synonyms": [
        {
            "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": "DOID:0111135",
            "label": "congenital generalized lipodystrophy type 1",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111136",
            "label": "congenital generalized lipodystrophy type 2",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111137",
            "label": "congenital generalized lipodystrophy type 3",
            "link_status": true,
            "children": []
        },
        {
            "id": "DOID:0111138",
            "label": "congenital generalized lipodystrophy type 4",
            "link_status": true,
            "children": []
        }
    ],
    "id_list": [
        "DOID:0111135",
        "DOID:0111136",
        "DOID:0050585",
        "DOID:0111137",
        "DOID:0111138"
    ],
    "unlinked_id_list": []
}