{
  "id": 9601,
  "label": "sporadic porphyria cutanea tarda",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008295",
  "properties": {
    "xrefs": [
      "GARD:0017749",
      "MEDGEN:357391",
      "MESH:C566768",
      "OMIM:176090",
      "Orphanet:443057",
      "SCTID:402479002",
      "UMLS:C1867968",
      "icd11.foundation:1813031784"
    ],
    "synonyms": [
      "acquired porphyria cutanea tarda",
      "porphyria cutanea tarda type I",
      "PCT, 'sporadic' type",
      "PCT, type 1",
      "porphyria cutanea tarda, type 1",
      "porphyria cutanea tarda, type I"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "An instance of porphyria cutanea tarda that is acquired during the lifetime of the individual."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16069,
      "label": "porphyria cutanea tarda",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496,
        4591
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3132",
          "GARD:0007433",
          "ICD10CM:E80.1",
          "MEDGEN:56453",
          "MESH:D017119",
          "MedDRA:10036183",
          "NANDO:1200816",
          "NANDO:2201267",
          "NCIT:C27725",
          "ONCOTREE:PCT",
          "Orphanet:101330",
          "SCTID:61860000",
          "UMLS:C0162566",
          "icd11.foundation:370983230"
        ],
        "synonyms": [
          "PCT",
          "porphyria cutania tarda"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "The most common form of chronic hepatic porphyria. It is characterized by bullous photodermatitis."
      },
      "child_count": 6,
      "reference_id": "MONDO:0015104"
    },
    {
      "id": 29231,
      "label": "acquired porphyria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7996,
        22990
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1853291",
          "UMLS:C0948592"
        ],
        "definition": "A porphyria disorder that is acquired during the lifetime of the individual."
      },
      "child_count": 2,
      "reference_id": "MONDO:1030015"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16069,
      "label": "porphyria cutanea tarda"
    },
    {
      "id": 29231,
      "label": "acquired porphyria"
    }
  ]
}