{
  "id": 10205,
  "label": "myoclonic cerebellar dyssynergia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008945",
  "properties": {
    "xrefs": [
      "DOID:12707",
      "EFO:1001053",
      "GARD:0009256",
      "MEDGEN:483579",
      "MESH:D002527",
      "OMIM:159700",
      "OMIM:213400",
      "SCTID:73495003",
      "UMLS:C3489626"
    ],
    "synonyms": [
      "cerebelloparenchymal disorder type 5",
      "dyssynergia cerebellaris myoclonica",
      "myoclonus and ataxia",
      "CPD5",
      "Ramsay Hunt cerebellar syndrome",
      "Ramsay Hunt syndrome",
      "Ramsay Hunt syndrome type 1",
      "Ramsay Hunt syndrome type 1 (formerly)",
      "Spinodentate atrophy",
      "cerebelloparenchymal disorder 5",
      "cerebelloparenchymal disorder V",
      "dentate cerebellar ataxia",
      "dentatorubral atrophy",
      "dyssynergia cerebellaris myoclonica of Hunt",
      "dyssynergia cerebellaris progressiva",
      "primary dentatum atrophy",
      "progressive myoclonus ataxia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A condition marked by progressive cerebellar ataxia combined with myoclonus usually presenting in the third decade of life or later. Additional clinical features may include generalized and focal seizures, spasticity, and dyskinesias. Autosomal recessive and autosomal dominant patterns of inheritance have been reported. Pathologically, the dentate nucleus and brachium conjunctivum of the cerebellum are atrophic, with variable involvement of the spinal cord, cerebellar cortex, and basal ganglia. (From Joynt, Clinical Neurology, 1991, Ch37, pp60-1)"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2729,
      "label": "cerebelloparenchymal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {},
      "child_count": 2,
      "reference_id": "MONDO:0000114"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020280",
          "MEDGEN:1825988",
          "MESH:D020271",
          "NCIT:C97073",
          "Orphanet:183500",
          "UMLS:C5680568"
        ],
        "synonyms": [
          "genetic neurodegenerative disease",
          "hereditary neurodegenerative disease",
          "hereditary neurodegenerative disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by progressive degeneration and atrophy of the nervous system."
      },
      "child_count": 164,
      "reference_id": "MONDO:0024237"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2729,
      "label": "cerebelloparenchymal disorder"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    }
  ]
}