{
    "disease_id": "DOID:11712",
    "recommended_name": {
        "id": "DOID:11712",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:11712",
        "name": "lipoatrophic diabetes mellitus",
        "description": "A type 2 diabetes mellitus that is characterized by severe insulin resistance and lipodystrophy."
    },
    "synonyms": [
        {
            "id": "DOID:11712",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11712",
            "name": "lipoatrophic diabetes",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "familial partial lipodystrophy, Dunnigan type",
            "description": "Familial Partial lipodystrophy, Dunnigan type (FPLD2) is a rare form of genetic lipodystrophy (see this term) characterized by a loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance, diabetes mellitus, dyslipidemia and liver steatosis."
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipoatrophic diabetes",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "reverse partial lipodystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipodystrophy, familial, of limbs and Lower trunk",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "Dunnigan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipodystrophy, reverse partial",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "familial lipodystrophy of limbs and lower trunk",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "familial partial lipodystrophy Dunnigan type",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "FPLD2",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipodystrophy, familial partial, type 2; FPLD2",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipodystrophy, familial partial, Dunnigan type",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "familial partial lipodystrophy type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "lipodystrophy, familial partial, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0007906",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007906",
            "name": "FPL2",
            "description": ""
        },
        {
            "id": "MIM:151660",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/151660",
            "name": "Lipodystrophy, familial partial, 2",
            "description": "Lipodystrophy, familial partial, 2"
        }
    ]
}