{
  "id": 24954,
  "label": "peroxisome biogenesis disorder, complementation group K",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800365",
  "properties": {
    "xrefs": [
      "GARD:0026524",
      "MEDGEN:356487",
      "UMLS:C1866257"
    ],
    "synonyms": [
      "CGK"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24006,
      "label": "peroxisome biogenesis disorder due to PEX14 defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19401
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026110"
        ],
        "synonyms": [
          "PEX14 related Zellweger spectrum disorder",
          "peroxisome biogenesis disorder due to PEX14 defect"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any Zellweger spectrum disorder in which the cause of the disease is a mutation in the PEX14 gene."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100268"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24006,
      "label": "peroxisome biogenesis disorder due to PEX14 defect"
    }
  ]
}