{
  "id": 18994,
  "label": "CANOMAD syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019109",
  "properties": {
    "xrefs": [
      "GARD:0009778",
      "MEDGEN:419872",
      "MESH:C537980",
      "Orphanet:71279",
      "SCTID:715624006",
      "UMLS:C2931684"
    ],
    "synonyms": [
      "chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome",
      "chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies",
      "chronic ataxic neuropathy ophthalmoplegia M-protein agglutination disialosyl antibodies syndrome",
      "chronic sensory ataxic neuropathy with anti-disialosyl antibodies"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "CANOMAD syndrome (Chronic Ataxic Neuropathy, Ophthalmoplegia, Monoclonal IgM protein, cold Agglutinins and Disialosyl antibodies) is a rare chronic immune-mediated demyelinating polyneuropathy."
  },
  "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"
    }
  ]
}