{
  "id": 22449,
  "label": "neuropathy, hereditary motor and sensory, type VIc, with optic atrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032792",
  "properties": {
    "xrefs": [
      "GARD:0025745",
      "MEDGEN:1680245",
      "OMIM:618511",
      "UMLS:C5193137"
    ],
    "synonyms": [
      "CMT 6C",
      "CMT6C",
      "Charcot-Marie-Tooth Disease, Type 6C",
      "HMSN 6C",
      "HMSN6C",
      "neuropathy, hereditary motor and sensory, type VIc, with optic atrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19358,
      "label": "hereditary motor and sensory neuropathy type 6",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16220
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080068",
          "GARD:0016787",
          "MEDGEN:140747",
          "Orphanet:90120",
          "UMLS:C0393807",
          "icd11.foundation:467894833"
        ],
        "synonyms": [
          "CMT6",
          "Charcot-Marie-Tooth disease type 6",
          "hereditary motor and sensory neuropathy type 6",
          "peripheral neuropathy and optic atrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0019551"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19358,
      "label": "hereditary motor and sensory neuropathy type 6"
    }
  ]
}