{
  "id": 13158,
  "label": "hereditary sensory and autonomic neuropathy type 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012092",
  "properties": {
    "xrefs": [
      "DOID:0070145",
      "GARD:0012328",
      "MEDGEN:6916",
      "OMIM:608654",
      "Orphanet:64752",
      "PMID:14976160",
      "PMID:77656",
      "SCTID:128206006",
      "UMLS:C0020075",
      "icd11.foundation:1411011731"
    ],
    "synonyms": [
      "HSAN5",
      "NGF autosomal recessive hereditary sensory and autonomic neuropathy",
      "autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF",
      "congenital insensitivity to pain and thermal analgesia",
      "hereditary sensory and autonomic neuropathy type V",
      "HSAN 5",
      "HSAN V",
      "insensitivity to pain, congenital",
      "neuropathy, hereditary sensory and autonomic, type 5",
      "neuropathy, hereditary sensory and autonomic, type V"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Hereditary sensory and autonomic neuropathy, type 5 (HSAN5) is characterized by loss of pain perception and impaired temperature sensitivity, in the absence of any other major neurological anomalies."
  },
  "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"
    }
  ]
}