{
  "id": 18898,
  "label": "multifocal motor neuropathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018979",
  "properties": {
    "xrefs": [
      "GARD:0011011",
      "ICD10CM:G61.82",
      "ICD9:357.89",
      "MEDGEN:581615",
      "NANDO:1200031",
      "NORD:1952",
      "Orphanet:641",
      "SCTID:230591002",
      "UMLS:C0393847"
    ],
    "synonyms": [
      "MMN",
      "MMNCB",
      "multifocal motor neuropathy with conduction block"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Multifocal motor neuropathy (MMN) is a rare acquired immune-mediatedneuropathy characterized clinically by a purely motor deficit with conduction block and asymmetric multifocal weakness, fasciculations, and cramping."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16613,
      "label": "acquired peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842976",
          "Orphanet:182086",
          "UMLS:C5680596"
        ],
        "synonyms": [
          "acquired peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of peripheral neuropathy that is acquired during the lifetime of the individual."
      },
      "child_count": 12,
      "reference_id": "MONDO:0015923"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16613,
      "label": "acquired peripheral neuropathy"
    }
  ]
}