{
    "disease_id": "DOID:0070204",
    "recommended_name": {
        "id": "DOID:0070204",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070204",
        "name": "familial partial lipodystrophy type 3",
        "description": "A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25."
    },
    "synonyms": [
        {
            "id": "DOID:0070204",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070204",
            "name": "familial partial lipodystrophy associated with PPARG mutations",
            "description": ""
        },
        {
            "id": "DOID:0070204",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070204",
            "name": "FPLD3",
            "description": ""
        },
        {
            "id": "DOID:0070204",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070204",
            "name": "PPARG-related FPLD",
            "description": ""
        },
        {
            "id": "DOID:0070204",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070204",
            "name": "PPARG-related familial partial lipodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "PPARG-related familial partial lipodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "FPLD3",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "PPARG-related FPLD",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "familial partial lipodystrophy type 3",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "familial partial lipodystrophy associated with PPARG mutations",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "insulin resistance, severe, digenic",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "lipodystrophy, familial partial, associated with Pparg mutations",
            "description": ""
        },
        {
            "id": "MONDO:0011448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011448",
            "name": "lipodystrophy, familial partial, type 3",
            "description": ""
        },
        {
            "id": "MIM:604367",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/604367",
            "name": "Lipodystrophy, familial partial, 3",
            "description": "Lipodystrophy, familial partial, 3"
        }
    ]
}