{
  "id": 14853,
  "label": "hereditary sensory and autonomic neuropathy type 6",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013839",
  "properties": {
    "xrefs": [
      "DOID:0070151",
      "GARD:0012987",
      "MEDGEN:761278",
      "OMIM:614653",
      "Orphanet:314381",
      "UMLS:C3539003"
    ],
    "synonyms": [
      "DST hereditary sensory and autonomic neuropathy",
      "HSAN6",
      "familial dysautonomia with contractures",
      "hereditary sensory and autonomic neuropathy caused by mutation in DST",
      "hereditary sensory and autonomic neuropathy type VI",
      "HSAN 6",
      "neuropathy, hereditary sensory and autonomic, type 6",
      "neuropathy, hereditary sensory and autonomic, type VI"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any hereditary sensory and autonomic neuropathy in which the cause of the disease is a mutation in the DST gene."
  },
  "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"
    }
  ]
}