{
  "id": 24916,
  "label": "xeroderma pigmentosum, type F/Cockayne syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800313",
  "properties": {
    "xrefs": [
      "GARD:0026496",
      "MEDGEN:812895",
      "UMLS:C3806565"
    ],
    "synonyms": [
      "XPF/CS"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16889,
      "label": "xeroderma pigmentosum-Cockayne syndrome complex",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        16625
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017130",
          "MEDGEN:930080",
          "NCIT:C156031",
          "Orphanet:220295",
          "UMLS:C4304411",
          "icd11.foundation:2002862606"
        ],
        "synonyms": [
          "XP/CS complex"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Xeroderma pigmentosum/Cockayne syndrome complex (XP/CS complex) is characterized by the cutaneous features of xeroderma pigmentosum (XP) together with the systemic and neurological features of Cockayne syndrome (CS)."
      },
      "child_count": 12,
      "reference_id": "MONDO:0016354"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16889,
      "label": "xeroderma pigmentosum-Cockayne syndrome complex"
    }
  ]
}