{
    "disease_id": "DOID:0070205", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "PLIN1-related familial partial lipodystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "familial partial lipodystrophy associated with PLIN1 mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "lipodystrophy, familial partial, type 4; FPLD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "PLIN1-related FPLD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "lipodystrophy, familial partial, type 4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "lipodystrophy, familial partial, associated with Plin1 mutations"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "FPLD4"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013478", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013478", 
            "name": "FPLD due to PLIN1 mutations"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070205", 
            "name": "FPLD4"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070205", 
            "name": "PLIN1-related FPLD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070205", 
            "name": "PLIN1-related familial partial lipodystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070205", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070205", 
            "name": "familial partial lipodystrophy associated with PLIN1 mutations"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070205", 
        "description": "A familial partial lipodystrophy characterized by autosomal dominant inheritance of loss of subcutaneous adipose tissue primarily from the lower limbs, insulin-resistant diabetes mellitus, hypertriglyceridemia, and hypertension that has_material_basis_in mutation in the PLIN1 gene on chromosome 15q26.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070205", 
        "name": "familial partial lipodystrophy type 4"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070205#disease-associations", 
            "id": "0070205", 
            "database": "Alliance of Genome Resources"
        }
    ]
}