{
  "id": 15431,
  "label": "LIPE-related familial partial lipodystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014431",
  "properties": {
    "xrefs": [
      "DOID:0070206",
      "GARD:0013126",
      "MEDGEN:863306",
      "OMIM:615980",
      "Orphanet:435660",
      "UMLS:C4014869"
    ],
    "synonyms": [
      "FPLD6",
      "LIPE-related FPLD",
      "familial partial lipodystrophy type 6",
      "lipodystrophy, familial partial, associated with Lipe mutations",
      "lipodystrophy, familial partial, type 6"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3144,
      "label": "abdominal obesity-metabolic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5777,
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060611",
          "ICD10CM:E88.81",
          "MEDGEN:419670",
          "MESH:C535554",
          "NCIT:C84442",
          "OMIMPS:605552",
          "Orphanet:411969",
          "UMLS:C2930930",
          "icd11.foundation:1824742930"
        ],
        "synonyms": [
          "metabolic syndrome",
          "metabolic syndrome X"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 15,
      "reference_id": "MONDO:0000816"
    },
    {
      "id": 19732,
      "label": "familial partial lipodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19731,
        20345,
        21770
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050440",
          "GARD:0011962",
          "MEDGEN:124408",
          "MESH:D052496",
          "NANDO:1200861",
          "NCIT:C84708",
          "NORD:1131",
          "OMIMPS:151660",
          "Orphanet:98306",
          "SCTID:49292002",
          "UMLS:C0271694",
          "icd11.foundation:1661968243"
        ],
        "synonyms": [
          "FPLD",
          "congenital partial lipodystrophy",
          "genetic partial lipodystrophy",
          "lipodystrophy, familial partial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Familial partial lipodystrophy (FPLD) is a group of rare genetic lipodystrophic syndromes characterized, in most cases, by fat loss from the limbs and buttocks, from childhood or early adulthood, and often associated with acanthosis nigricans, insulin resistance, diabetes, hypertriglyceridemia and liver steatosis."
      },
      "child_count": 30,
      "reference_id": "MONDO:0020088"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3144,
      "label": "abdominal obesity-metabolic syndrome"
    },
    {
      "id": 19732,
      "label": "familial partial lipodystrophy"
    }
  ]
}