{
    "disease_id": "DOID:0070204", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "PPARG-related familial partial lipodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "lipodystrophy, familial partial, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "PPARG-related FPLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "familial partial lipodystrophy associated with PPARG mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "FPLD3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "lipodystrophy, familial partial, associated with Pparg mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011448", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011448", 
            "name": "lipodystrophy, familial partial, type 3; FPLD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070204", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070204", 
            "name": "familial partial lipodystrophy associated with PPARG mutations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070204", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070204", 
            "name": "FPLD3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070204", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070204", 
            "name": "PPARG-related FPLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070204", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070204", 
            "name": "PPARG-related familial partial lipodystrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070204", 
        "description": "A familial partial lipodystrophy characterized by autosomal dominant inheritance that has_material_basis_in mutation in the PPARG gene on chromosome 3p25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070204", 
        "name": "familial partial lipodystrophy type 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070204#disease-associations", 
            "id": "0070204", 
            "database": "Alliance of Genome Resources"
        }
    ]
}