{
  "id": 15290,
  "label": "neuropathy, hereditary sensory, type 1F",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014286",
  "properties": {
    "xrefs": [
      "DOID:0070154",
      "GARD:0015995",
      "MEDGEN:816524",
      "OMIM:615632",
      "UMLS:C3810194"
    ],
    "synonyms": [
      "ATL3 hereditary sensory and autonomic neuropathy type 1",
      "HSN1F",
      "hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3",
      "neuropathy, hereditary sensory, type 1F",
      "HSN 1F",
      "hereditary sensory neuropathy type 1F",
      "neuropathy, hereditary sensory, type IF"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any hereditary sensory and autonomic neuropathy type 1 in which the cause of the disease is a mutation in the ATL3 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18346,
      "label": "hereditary sensory and autonomic neuropathy type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16223,
        18270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070162",
          "GARD:0006635",
          "MEDGEN:5645",
          "NORD:1237",
          "Orphanet:36386",
          "PMID:18348718",
          "SCTID:397734008",
          "UMLS:C0020071",
          "icd11.foundation:1989773046"
        ],
        "synonyms": [
          "HSAN1",
          "Hereditary Sensory Neuropathy Type I",
          "hereditary sensory and autonomic neuropathy type I",
          "HSAN 1",
          "HSN1",
          "hereditary sensory neuropathy type 1",
          "neuropathy hereditary sensory and autonomic type 1",
          "neuropathy hereditary sensory radicular, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Hereditary sensory neuropathy type I (HSN I) is a slowly progressive neurological disorder characterized by prominent predominantly distal sensory loss, autonomic disturbances, autosomal dominant inheritance, and juvenile or adulthood disease onset."
      },
      "child_count": 12,
      "reference_id": "MONDO:0018213"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18346,
      "label": "hereditary sensory and autonomic neuropathy type 1"
    }
  ]
}