{
  "id": 7462,
  "label": "Miller Fisher syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005851",
  "properties": {
    "xrefs": [
      "DOID:12889",
      "EFO:0007371",
      "GARD:0003668",
      "MEDGEN:95994",
      "MESH:D019846",
      "MedDRA:10049567",
      "NCIT:C116958",
      "Orphanet:98919",
      "SCTID:1767005",
      "UMLS:C0393799",
      "icd11.foundation:134795253"
    ],
    "synonyms": [
      "Fisher syndrome",
      "Guillain Barre syndrome, Miller Fisher variant",
      "Guillain-Barre syndrome, Miller Fisher variant",
      "Miller Fisher variant of Guillain Barre syndrome",
      "Miller-Fisher syndrome",
      "cranial variant of GBS",
      "cranial variant of Guillain-Barre syndrome",
      "cranial variant of Guillain-Barré syndrome",
      "ophthalmoplegia, ataxia and areflexia syndrome",
      "syndrome, Fisher",
      "syndrome, Miller Fisher",
      "syndrome, Miller-Fisher"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An autoimmune process characterized by the clinical triad of ophthalmoplegia, ataxia, and areflexia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2996,
      "label": "autoimmune disorder of central nervous system",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657,
        4981
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060004",
          "EFO:0020092"
        ],
        "synonyms": [
          "central nervous system autoimmune disease",
          "central nervous system hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hypersensitivity reaction type II disease that involves the central nervous system."
      },
      "child_count": 16,
      "reference_id": "MONDO:0000568"
    },
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 4515,
      "label": "cerebellar disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2786",
          "MEDGEN:40186",
          "MESH:D002526",
          "SCTID:223176004",
          "UMLS:C0007760"
        ],
        "synonyms": [
          "cerebellum disease",
          "cerebellum disease or disorder",
          "disease of cerebellum",
          "disease or disorder of cerebellum",
          "disorder of cerebellum"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, gait ataxia, and muscle hypotonia."
      },
      "child_count": 5,
      "reference_id": "MONDO:0002427"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2996,
      "label": "autoimmune disorder of central nervous system"
    },
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 4515,
      "label": "cerebellar disorder"
    }
  ]
}