{
  "id": 14600,
  "label": "Keppen-Lubinsky syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013572",
  "properties": {
    "xrefs": [
      "GARD:0017716",
      "MEDGEN:481430",
      "OMIM:614098",
      "Orphanet:435628",
      "UMLS:C3279800"
    ],
    "synonyms": [
      "Keppen-Lubinsky syndrome",
      "generalised lipodystrophy-progeroid features-severe intellectual disability syndrome",
      "generalized lipodystrophy-progeroid features-severe intellectual disability syndrome",
      "KEPPEN-Lubinsky syndrome",
      "KPLBS"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19731,
      "label": "hereditary lipodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8053,
        18954,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012597",
          "MEDGEN:1383706",
          "Orphanet:98305",
          "SCTID:724841000",
          "UMLS:C4511302",
          "icd11.foundation:1166232738"
        ],
        "synonyms": [
          "genetic lipodystrophy",
          "genetic lipodystrophy (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of lipodystrophy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 33,
      "reference_id": "MONDO:0020087"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19731,
      "label": "hereditary lipodystrophy"
    }
  ]
}