{
  "id": 21165,
  "label": "foix chavany Marie syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023171",
  "properties": {
    "xrefs": [
      "GARD:0002351",
      "MEDGEN:419406",
      "MESH:C537069",
      "Orphanet:2048",
      "SCTID:720956003",
      "UMLS:C2931412"
    ],
    "synonyms": [
      "foix chavany Marie syndrome",
      "anterior opercular syndrome",
      "bilateral anterior opercular syndrome",
      "congenital Foix-Chavany-Marie syndrome",
      "congenital Foix-Chavany-Marie syndrome (subtype)",
      "facio-Labio-pharyngo-Glosso-laryngo-brachial paralysis",
      "facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation",
      "facio-pharyngo-glosso-masticatory diplegia",
      "opercular syndrome, anterior",
      "pseudobulbar paralysis, cortical type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Foix-Chavany-Marie syndrome (FCMS) is a cortico-subcortical suprabulbar or pseudobulbar palsy of the lower cranial nerves, characterized by severe dysarthria and dysphagia associated with bilateral central facio-pharyngo-glosso-masticatory paralysis, with prominent automatic-voluntary dissociation in which involuntary movements of the affected muscles are preserved."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4000,
      "label": "multiple cranial nerve palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4811
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13866",
          "ICD9:352.6",
          "MEDGEN:509636",
          "SCTID:78152008",
          "UMLS:C0154733"
        ],
        "synonyms": [
          "multiple cranial nerve palsies"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0001819"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4000,
      "label": "multiple cranial nerve palsy"
    },
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}