{
  "id": 10957,
  "label": "hereditary sensory and autonomic neuropathy type 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009746",
  "properties": {
    "xrefs": [
      "DOID:0070146",
      "GARD:0003006",
      "MEDGEN:6915",
      "NANDO:1200553",
      "NANDO:2200854",
      "NCIT:C118633",
      "NORD:1236",
      "OMIM:256800",
      "Orphanet:642",
      "PMID:14272277",
      "PMID:8696348",
      "SCTID:62985007",
      "UMLS:C0020074",
      "icd11.foundation:1831234152"
    ],
    "synonyms": [
      "CIP-anhidrosis syndrome",
      "HSAN4",
      "Hereditary Sensory and Autonomic Neuropathy Type IV",
      "NTRK1 hereditary sensory and autonomic neuropathy",
      "congenital insensitivity to pain with anhidrosis",
      "congenital insensitivity to pain-anhidrosis syndrome",
      "hereditary sensory and autonomic neuropathy caused by mutation in NTRK1",
      "hereditary sensory and autonomic neuropathy type IV",
      "insensitivity to pain, congenital, with anhidrosis",
      "CIPA",
      "HSAN 4",
      "HSAN IV",
      "HSNAN4",
      "familial dysautonomia, type 2",
      "hereditary sensory and autonomic neuropathy 4",
      "hereditary sensory neuropathy type 4",
      "neuropathy, congenital sensory, with anhidrosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Hereditary sensory and autonomic neuropathy, type 4 (HSAN4) is an inherited disorder characterized by anhidrosis, insensitivity to pain, self-mutilating behavior and episodes of fever."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16223,
      "label": "hereditary sensory and autonomic neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4428,
        19748
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050548",
          "GARD:0012688",
          "ICD9:356.2",
          "MEDGEN:14355",
          "MESH:D009477",
          "NCIT:C125386",
          "OMIMPS:162400",
          "Orphanet:140471",
          "SCTID:11442006",
          "UMLS:C0027889",
          "icd11.foundation:1091217288"
        ],
        "synonyms": [
          "CIP",
          "HSAN",
          "congenital insensitivity to pain",
          "congenital pain insensitivity",
          "hereditary sensory and autonomic neuropathy",
          "hereditary sensory neuropathy",
          "hereditary sensory peripheral neuropathy",
          "indifference to pain, Congenital, autosomal recessive",
          "hereditary sensory autonomic neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of sensory peripheral neuropathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 26,
      "reference_id": "MONDO:0015364"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16223,
      "label": "hereditary sensory and autonomic neuropathy"
    }
  ]
}