{
    "disease_id": "DOID:0070205",
    "recommended_name": {
        "id": "DOID:0070205",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070205",
        "name": "familial partial lipodystrophy type 4",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0070205",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070205",
            "name": "FPLD4",
            "description": ""
        },
        {
            "id": "DOID:0070205",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070205",
            "name": "PLIN1-related FPLD",
            "description": ""
        },
        {
            "id": "DOID:0070205",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070205",
            "name": "PLIN1-related familial partial lipodystrophy",
            "description": ""
        },
        {
            "id": "DOID:0070205",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070205",
            "name": "familial partial lipodystrophy associated with PLIN1 mutations",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "PLIN1-related familial partial lipodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "familial partial lipodystrophy associated with PLIN1 mutations",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "familial partial lipodystrophy type 4",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "lipodystrophy, familial partial, type 4; FPLD4",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "PLIN1-related FPLD",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "lipodystrophy, familial partial, type 4",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "lipodystrophy, familial partial, associated with Plin1 mutations",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "FPLD4",
            "description": ""
        },
        {
            "id": "MONDO:0013478",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013478",
            "name": "FPLD due to PLIN1 mutations",
            "description": ""
        },
        {
            "id": "MIM:613877",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613877",
            "name": "Lipodystrophy, familial partial, 4",
            "description": "Lipodystrophy, familial partial, 4"
        }
    ]
}