{
  "id": 8677,
  "label": "carpal tunnel syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007275",
  "properties": {
    "xrefs": [
      "DOID:12169",
      "EFO:0004143",
      "GARD:0027775",
      "ICD10CM:G56.0",
      "ICD9:354.0",
      "MEDGEN:2856",
      "MESH:D002349",
      "NCIT:C34450",
      "OMIMPS:115430",
      "Orphanet:50838",
      "SCTID:57406009",
      "UMLS:C0007286",
      "icd11.foundation:1275186848"
    ],
    "synonyms": [
      "carpal tunnel syndrome",
      "CTS",
      "amyotrophy, thenar, of carpal origin"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Entrapment of the median nerve in the wrist that is characterized by numbness, tingling and painful movement."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 5507,
      "label": "nerve compression syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:573",
          "EFO:0009487",
          "MEDGEN:266933",
          "MESH:D009408",
          "NCIT:C27221",
          "SCTID:45781009",
          "UMLS:C1510429"
        ],
        "synonyms": [
          "entrapment neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any nerve disorder caused by the entrapment and compression of a nerve."
      },
      "child_count": 3,
      "reference_id": "MONDO:0003615"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010711",
          "MEDGEN:1825937",
          "Orphanet:98497",
          "UMLS:C5681733"
        ],
        "synonyms": [
          "genetic peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 130,
      "reference_id": "MONDO:0020127"
    }
  ],
  "children": [
    {
      "id": 20136,
      "label": "carpal tunnel syndrome 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8677
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070466",
          "GARD:0025228",
          "MEDGEN:1830382",
          "OMIM:115430",
          "UMLS:C5779776"
        ],
        "synonyms": [
          "carpal tunnel syndrome",
          "CTS1",
          "amyotrophy, thenar, of carpal origin",
          "carpal tunnel syndrome, familial",
          "CTS"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020730"
    },
    {
      "id": 22094,
      "label": "carpal tunnel syndrome 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        8677
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070467",
          "GARD:0025650",
          "MEDGEN:1725962",
          "OMIM:619161",
          "UMLS:C5436916"
        ],
        "synonyms": [
          "CTS2",
          "carpal tunnel syndrome 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030883"
    }
  ],
  "roots": [
    {
      "id": 5507,
      "label": "nerve compression syndrome"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy"
    }
  ]
}