{
  "id": 15107,
  "label": "CIDEC-related familial partial lipodystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014098",
  "properties": {
    "xrefs": [
      "DOID:0070203",
      "GARD:0013125",
      "MEDGEN:815270",
      "OMIM:615238",
      "Orphanet:435651",
      "UMLS:C3808940"
    ],
    "synonyms": [
      "CIDEC-related FPLD",
      "CIDEC-related familial partial lipodystrophy",
      "FPLD5",
      "lipodystrophy, familial partial, associated with Cidec mutations",
      "lipodystrophy, familial partial, type 5"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 19732,
      "label": "familial partial lipodystrophy"
    }
  ]
}