{
  "id": 25727,
  "label": "variegate porphyria, childhood-onset",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0957577",
  "properties": {
    "xrefs": [
      "GARD:0026867",
      "MEDGEN:1849794",
      "OMIM:620483",
      "UMLS:C5882681"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9603,
      "label": "variegate porphyria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24756
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4346",
          "GARD:0007848",
          "MEDGEN:58118",
          "MESH:D046350",
          "NANDO:1200814",
          "NANDO:2201265",
          "NCIT:C85219",
          "NORD:1821",
          "OMIM:176200",
          "Orphanet:79473",
          "SCTID:58275005",
          "UMLS:C0162532",
          "icd11.foundation:1227474618"
        ],
        "synonyms": [
          "Protocoproporphyria",
          "protoporphyrinogen oxidase deficiency",
          "variegate porphyria",
          "PPOX deficiency",
          "VP",
          "porphyria variegata",
          "porphyria variegata, susceptibility to",
          "porphyria variegate",
          "porphyria, South African type",
          "variegate porphyria, homozygous variant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Variegate porphyria is a form of acute hepatic porphyria characterized by the occurrence of neuro-visceral attacks with or without the presence of cutaneous lesions."
      },
      "child_count": 1,
      "reference_id": "MONDO:0008297"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9603,
      "label": "variegate porphyria"
    }
  ]
}