{
  "id": 14962,
  "label": "peroxisome biogenesis disorder 12A (Zellweger)",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013951",
  "properties": {
    "xrefs": [
      "DOID:0080486",
      "GARD:0015876",
      "MEDGEN:766916",
      "OMIM:614886",
      "UMLS:C3554002"
    ],
    "synonyms": [
      "peroxisome biogenesis disorder 12A (Zellweger)",
      "Cg14",
      "Cgj",
      "PBD12A",
      "peroxisome biogenesis disorder, complementation group 14",
      "peroxisome biogenesis disorder, complementation group J"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24008,
      "label": "peroxisome biogenesis disorder due to PEX19 defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19401
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026112"
        ],
        "synonyms": [
          "PEX19 related Zellweger spectrum disorder",
          "peroxisome biogenesis disorder due to PEX19 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 PEX19 gene."
      },
      "child_count": 1,
      "reference_id": "MONDO:0100270"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24008,
      "label": "peroxisome biogenesis disorder due to PEX19 defect"
    }
  ]
}