{
    "disease_id": "DOID:0070206", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "LIPE-related familial partial lipodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "FPLD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "lipodystrophy, familial partial, type 6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "LIPE-related FPLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "lipodystrophy, familial partial, associated with Lipe mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "lipodystrophy, familial partial, type 6; FPLD6"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014431", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014431", 
            "name": "familial partial lipodystrophy associated with LIPE mutations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070206", 
            "name": "familial partial lipodystrophy associated with LIPE mutations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070206", 
            "name": "FPLD6"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070206", 
            "name": "LIPE-related FPLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070206", 
            "name": "LIPE-related familial partial lipodystrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070206", 
        "description": "A familial partial lipodystrophy characterized by autosomal recessive inheritance that has_material_basis_in mutation in the LIPE gene on chromosome 19q13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070206", 
        "name": "familial partial lipodystrophy type 6"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070206#disease-associations", 
            "id": "0070206", 
            "database": "Alliance of Genome Resources"
        }
    ]
}
