{
  "id": 6741,
  "label": "chronic pancreatitis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005003",
  "properties": {
    "xrefs": [
      "DOID:0051065",
      "EFO:0000342",
      "ICD9:577.1",
      "MEDGEN:101753",
      "MESH:D050500",
      "NCIT:C84637",
      "SCTID:235494005",
      "UMLS:C0149521",
      "icd11.foundation:1758007371"
    ],
    "synonyms": [
      "pancreatitis, chronic"
    ],
    "categories": [
      {
        "ref": "MONDO:0004335",
        "name": "digestive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A chronic inflammatory process causing damage and fibrosis of the pancreatic parenchyma. Signs and symptoms include abdominal pain, malabsorption and diabetes mellitus."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 6723,
      "label": "pancreatitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4455,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4989",
          "EFO:0000278",
          "MEDGEN:14586",
          "MESH:D010195",
          "NCIT:C3306",
          "SCTID:75694006",
          "UMLS:C0030305"
        ],
        "synonyms": [
          "inflammation of pancreas",
          "pancreas inflammation"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Inflammation of the pancreas."
      },
      "child_count": 10,
      "reference_id": "MONDO:0004982"
    }
  ],
  "children": [
    {
      "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"
    },
    {
      "id": 17566,
      "label": "autoimmune pancreatitis type 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6741,
        16099
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1000780",
          "GARD:0021076",
          "MEDGEN:927912",
          "Orphanet:280302",
          "PMID:25985088",
          "SCTID:722872000",
          "UMLS:C4302243"
        ],
        "synonyms": [
          "AIP type 1",
          "IgG4-related pancreatitis",
          "autoimmune pancreatitis type 1",
          "lymphoplasmacytic sclerosing pancreatitis"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Type 1 autoimmune pancreatitis is a form of autoimmune pancreatitis seen in elderly males (>60 years) and presenting with abdominal pain, steatorrhea, obstructive jaundice and other organ (bile duct, kidneys and retroperitoneum) involvement. It is thought to be due to an immunoglobulin G4 (IgG4)-associated systemic disease."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017227"
    },
    {
      "id": 26305,
      "label": "idiopathic chronic pancreatitis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6741
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:574410",
          "Orphanet:700133",
          "UMLS:C0341471"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0979357"
    }
  ],
  "roots": [
    {
      "id": 6723,
      "label": "pancreatitis"
    }
  ]
}