{
  "id": 15666,
  "label": "neuropathy, hereditary motor and sensory, type 6B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014671",
  "properties": {
    "xrefs": [
      "GARD:0018092",
      "MEDGEN:895482",
      "OMIM:616505",
      "UMLS:C4225302"
    ],
    "synonyms": [
      "CMT6B",
      "Charcot-Marie-Tooth disease, type 6B",
      "HMSN 6B",
      "HMSN6B",
      "SLC25A46 hereditary motor and sensory neuropathy type 6",
      "hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46",
      "neuropathy, hereditary motor and sensory, type 6B",
      "neuropathy, hereditary motor and sensory, type VIB"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any hereditary motor and sensory neuropathy type 6 in which the cause of the disease is a mutation in the SLC25A46 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4423,
      "label": "motor peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2477",
          "ICD9:356.9",
          "MEDGEN:82885",
          "NCIT:C3500",
          "SCTID:95663000",
          "UMLS:C0271683"
        ],
        "synonyms": [
          "peripheral motor neuropathy",
          "HSMN",
          "HSMN - hereditary sensory and motor neuropathy",
          "hereditary motor and sensory neuropathy",
          "neuropathic muscular atrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Inflammation or degeneration of the peripheral motor nerves."
      },
      "child_count": 9,
      "reference_id": "MONDO:0002316"
    },
    {
      "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": 4423,
      "label": "motor peripheral neuropathy"
    },
    {
      "id": 19358,
      "label": "hereditary motor and sensory neuropathy type 6"
    }
  ]
}