{
  "id": 3545,
  "label": "chondrocalcinosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001314",
  "properties": {
    "xrefs": [
      "DOID:1156",
      "HP:0000934",
      "ICD9:275.49",
      "ICD9:712.1",
      "MEDGEN:154303",
      "MESH:D002805",
      "NCIT:C34955",
      "SCTID:239832006",
      "UMLS:C0553730",
      "icd11.foundation:2041797033"
    ],
    "synonyms": [
      "calcium pyrophosphate deposition disease",
      "pseudogout"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "An acute episode of pain, swelling, and redness, sometimes associated with fever. It is caused by the deposition of calcium pyrophosphate crystals in the joints."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 6795,
      "label": "metabolic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0014667",
          "EFO:0000589",
          "ICD10CM:E70-E88",
          "ICD10WHO:E70-E90",
          "ICD9:277.8",
          "ICD9:277.9",
          "MEDGEN:44376",
          "MESH:D008659",
          "NANDO:1100002",
          "NCIT:C3235",
          "SCTID:75934005",
          "UMLS:C0025517"
        ],
        "synonyms": [
          "disorder of metabolic process",
          "metabolic disease",
          "metabolic disorder",
          "metabolic process disease",
          "disease of metabolism"
        ],
        "definition": "A congenital disorder (due to inherited enzyme abnormality) or acquired (due to failure of a metabolically important organ) disorder resulting from an abnormal metabolic process."
      },
      "child_count": 37,
      "reference_id": "MONDO:0005066"
    },
    {
      "id": 7223,
      "label": "arthritic joint disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4665,
        8264,
        20399
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:848",
          "EFO:0005856",
          "MEDGEN:2043",
          "MESH:D001168",
          "NCIT:C2883",
          "SCTID:3723001",
          "UMLS:C0003864",
          "Wikipedia:Arthritis"
        ],
        "synonyms": [
          "arthritis",
          "inflammation of skeletal joint",
          "skeletal joint inflammation",
          "inflammatory disorder of joint"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An inflammatory process affecting a joint. Causes include infection, autoimmune processes, degenerative processes, and trauma. Signs and symptoms may include swelling around the affected joint and pain."
      },
      "child_count": 39,
      "reference_id": "MONDO:0005578"
    },
    {
      "id": 25070,
      "label": "metabolic bone disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7061
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:2699",
          "NCIT:C97045",
          "UMLS:C0005944"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A group of disorders that affect the bones secondary to increased levels of minerals or deficient levels of minerals such as calcium, magnesium, phosphorus, and vitamin D. Representative examples are osteomalacia, osteoporosis, and Paget disease."
      },
      "child_count": 4,
      "reference_id": "MONDO:0800486"
    }
  ],
  "children": [
    {
      "id": 8717,
      "label": "chondrocalcinosis 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3545,
        7203,
        18954,
        21247,
        24807
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001292",
          "MEDGEN:163633",
          "MESH:C563162",
          "NORD:930",
          "OMIM:118600",
          "Orphanet:1416",
          "UMLS:C0856830"
        ],
        "synonyms": [
          "Familial Calcium Pyrophosphate Deposition Disease",
          "calcium pyrophosphate dihydrate crystal deposition disease",
          "chondrocalcinosis 2",
          "chondrocalcinosis type 2",
          "familial CC",
          "familial CPPD",
          "familial articular chondrocalcinosis",
          "familial calcium pyrophosphate deposition",
          "familial calcium pyrophosphate dihydrate deposition disease",
          "hereditary CC",
          "hereditary articular chondrocalcinosis",
          "hereditary calcium pyrophosphate deposition",
          "CCAL2",
          "CPPDD",
          "Pseudogout, familial",
          "calcium gout",
          "calcium gout, familial",
          "calcium pyrophosphate arthropathy",
          "calcium pyrophosphate arthropathy, familial",
          "calcium pyrophosphate dihydrate deposition disease",
          "chondrocalcinosis familial articular",
          "chondrocalcinosis, familial articular"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "A chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calcium pyrophosphate (CPP) crystal arthritis and polyarticular osteoarthritis (OA)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007319"
    },
    {
      "id": 8718,
      "label": "chondrocalcinosis due to apatite crystal deposition",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3545
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:349317",
          "MESH:C535939",
          "OMIM:118610",
          "UMLS:C1861580"
        ],
        "synonyms": [
          "chondrocalcinosis due to apatite crystal deposition",
          "familial apatite disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007320"
    },
    {
      "id": 12050,
      "label": "chondrocalcinosis 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3545
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0006048",
          "MEDGEN:331527",
          "MESH:C535938",
          "OMIM:600668",
          "UMLS:C1833499"
        ],
        "synonyms": [
          "CCAL1",
          "chondrocalcinosis 1",
          "chondrocalcinosis with early-onset osteoarthritis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010917"
    }
  ],
  "roots": [
    {
      "id": 6795,
      "label": "metabolic disease"
    },
    {
      "id": 7223,
      "label": "arthritic joint disease"
    },
    {
      "id": 25070,
      "label": "metabolic bone disorder"
    }
  ]
}