{
  "id": 13057,
  "label": "tropical pancreatitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011986",
  "properties": {
    "xrefs": [
      "GARD:0016946",
      "MEDGEN:334069",
      "MESH:C564276",
      "OMIM:608189",
      "Orphanet:103918",
      "SCTID:724540009",
      "UMLS:C1842402",
      "icd11.foundation:1645607956"
    ],
    "synonyms": [
      "TCP",
      "tropical calcific chronic pancreatitis",
      "fibrocalculous pancreatic diabetes, susceptibility to",
      "tropical calcific pancreatitis"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Tropical pancreatitis is a rare pancreatic disease of juvenile onset occurring mainly in tropical developing countries and characterized by chronic non-alcoholic pancreatitis manifesting with abdominal pain, steatorrhea and fibrocalculous pancreatopathy. It is also commonly associated with the development of pancreatic calculi and pancreatic cancer at a much higher frequency than seen in ordinary chronic pancreatitis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9496,
      "label": "hereditary chronic pancreatitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6741
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006632",
          "ICD9:577.8",
          "MEDGEN:116056",
          "MESH:C537262",
          "NANDO:1200921",
          "NANDO:2200942",
          "NCIT:C95436",
          "OMIM:167800",
          "Orphanet:676",
          "SCTID:68072000",
          "UMLS:C0238339",
          "icd11.foundation:1287702961"
        ],
        "synonyms": [
          "hereditary chronic pancreatitis",
          "hereditary pancreatitis",
          "HPC",
          "Hp",
          "PCTT",
          "autosomal dominant hereditary pancreatitis",
          "familial pancreatitis",
          "pancreatitis, calcific",
          "pancreatitis, calcific, included",
          "pancreatitis, chronic",
          "pancreatitis, chronic pancreatitis, chronic, susceptibility to, included",
          "pancreatitis, chronic, protection against",
          "pancreatitis, chronic, protection against, included",
          "pancreatitis, chronic, susceptibility to",
          "pancreatitis, hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Hereditary chronic pancreatitis (HCP), a rare inherited form of pancreatitis is defined as recurrent acute pancreatitis and/or chronic pancreatitis in two first-degree relatives or 3 or more second-degree relatives in 2 or more generations, for which no predisposing factors are identified. HCP is characterized by irreversible damage to both exocrine and endocrine components of the pancreas."
      },
      "child_count": 4,
      "reference_id": "MONDO:0008185"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9496,
      "label": "hereditary chronic pancreatitis"
    }
  ]
}