{
  "id": 4235,
  "label": "facial nerve disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002098",
  "properties": {
    "xrefs": [
      "DOID:1756",
      "EFO:1002051",
      "ICD10CM:G51",
      "ICD9:351",
      "ICD9:351.9",
      "MEDGEN:41946",
      "MESH:D005155",
      "NCIT:C27594",
      "SCTID:422426003",
      "UMLS:C0015464"
    ],
    "synonyms": [
      "disease of facial nerve",
      "disease or disorder of facial nerve",
      "disorder of facial nerve",
      "facial nerve disease",
      "facial nerve disease or disorder",
      "facial nerve disorder",
      "disorder of seventh cranial nerve",
      "disorders of the VIIth cranial nerve",
      "disorders of the seventh nerve",
      "facial neuropathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A disease involving the facial nerve."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 9,
  "parents": [
    {
      "id": 5469,
      "label": "cranial nerve neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5656",
          "ICD9:352.9",
          "MEDGEN:1160",
          "MESH:D003389",
          "NCIT:C26733",
          "SCTID:73013002",
          "UMLS:C0010266"
        ],
        "synonyms": [
          "cranial nerve disease",
          "cranial nerve disorder",
          "cranial neuron projection bundle disease",
          "cranial neuron projection bundle disease or disorder",
          "cranial neuropathy",
          "disease of cranial neuron projection bundle",
          "disease or disorder of cranial neuron projection bundle",
          "disorder of cranial nerve",
          "disorder of cranial neuron projection bundle"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplastic or non-neoplastic disorder that affects one of the cranial nerves."
      },
      "child_count": 17,
      "reference_id": "MONDO:0003569"
    },
    {
      "id": 5512,
      "label": "peripheral nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:574",
          "EFO:0009387",
          "ICD9:350-359",
          "ICD9:356.9",
          "MEDGEN:892389",
          "MESH:D010523",
          "NCIT:C27580",
          "SCTID:42658009",
          "UMLS:C4025831"
        ],
        "synonyms": [
          "PNS (peripheral nervous system) diseases",
          "PNS disease",
          "PNS diseases",
          "disease of peripheral nervous system",
          "disease or disorder of peripheral nervous system",
          "disorder of peripheral nervous system",
          "disorder of the peripheral nervous system",
          "peripheral nervous system disease",
          "peripheral nervous system disease or disorder",
          "peripheral nervous system disorder",
          "peripheral nervous system disorders",
          "nerve disease, peripheral",
          "nerve diseases, peripheral",
          "neuropathy, peripheral",
          "peripheral Neuropathies",
          "peripheral nerve disease",
          "peripheral nerve diseases",
          "peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease involving the peripheral nervous system."
      },
      "child_count": 18,
      "reference_id": "MONDO:0003620"
    }
  ],
  "children": [
    {
      "id": 3999,
      "label": "facial neuralgia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        16906
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13865",
          "EFO:0009380",
          "GARD:0023014",
          "ICD9:351.8",
          "MEDGEN:5099",
          "MESH:D005156",
          "SCTID:4151000119102",
          "UMLS:C0015467"
        ],
        "synonyms": [
          "facial nerve neuralgia",
          "neuralgia of facial nerve"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neuralgic syndromes which feature chronic or recurrent facial pain as the primary manifestation of disease. Disorders of the trigeminal and facial nerves are frequently associated with these conditions."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001818"
    },
    {
      "id": 4048,
      "label": "geniculate ganglionitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        20399,
        20464
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14075",
          "ICD10CM:G51.1",
          "ICD9:351.1",
          "MEDGEN:4879",
          "SCTID:72839009",
          "UMLS:C0017407",
          "icd11.foundation:305361524"
        ],
        "synonyms": [
          "geniculate ganglion inflammation",
          "geniculate ganglionitis",
          "inflammation of geniculate ganglion"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Diseases of the facial nerve or nuclei. Pontine disorders may affect the facial nuclei or nerve fascicle. The nerve may be involved intracranially, along its course through the petrous portion of the temporal bone, or along its extracranial course. Clinical manifestations include facial muscle weakness, loss of taste from the anterior tongue, hyperacusis, and decreased lacrimation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001873"
    },
    {
      "id": 4238,
      "label": "facial nerve neoplasm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        4684
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1760",
          "ICD9:239.7",
          "MEDGEN:224733",
          "NCIT:C5827",
          "SCTID:126973004",
          "UMLS:C1263899"
        ],
        "synonyms": [
          "VIIth cranial nerve neoplasms",
          "VIIth cranial nerve tumors",
          "VIIth cranial nerve tumours",
          "facial nerve neoplasm",
          "facial nerve neoplasm (disease)",
          "facial nerve neoplasms",
          "facial nerve tumor",
          "facial nerve tumors",
          "facial nerve tumour",
          "facial nerve tumours",
          "neoplasm of Facial nerve",
          "neoplasm of facial nerve",
          "neoplasm of seventh cranial nerve",
          "neoplasm of the Facial nerve",
          "neoplasm of the seventh cranial nerve",
          "seventh cranial nerve neoplasm",
          "seventh cranial nerve neoplasms",
          "seventh cranial nerve tumor",
          "seventh cranial nerve tumors",
          "seventh cranial nerve tumour",
          "seventh cranial nerve tumours",
          "tumor of Facial nerve",
          "tumor of facial nerve",
          "tumor of seventh cranial nerve",
          "tumor of the Facial nerve",
          "tumor of the seventh cranial nerve",
          "tumour of Facial nerve",
          "tumour of facial nerve",
          "tumour of seventh cranial nerve",
          "tumour of the Facial nerve",
          "tumour of the seventh cranial nerve"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neoplasm involving a facial nerve."
      },
      "child_count": 0,
      "reference_id": "MONDO:0002101"
    },
    {
      "id": 7300,
      "label": "Bell's palsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4015,
        4235,
        4811
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12506",
          "EFO:0007167",
          "ICD10CM:G51.0",
          "ICD9:351.0",
          "MEDGEN:87660",
          "MESH:D020330",
          "NCIT:C26769",
          "Orphanet:2810",
          "SCTID:193093009",
          "UMLS:C0376175"
        ],
        "synonyms": [
          "facial nerve palsy",
          "facial nerve paralysis",
          "nerve paralysis, Facial",
          "palsy of facial nerve",
          "paralysis Of Facial nerve",
          "facial palsy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Partial or complete paralysis of the facial muscles of one side of a person's face. It is caused by damage to the seventh cranial nerve. It is usually temporary but it may recur."
      },
      "child_count": 3,
      "reference_id": "MONDO:0005665"
    },
    {
      "id": 9064,
      "label": "facial hemiatrophy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1757",
          "GARD:0007338",
          "MEDGEN:8761",
          "MESH:D005150",
          "NCIT:C116916",
          "OMIM:141300",
          "Orphanet:1214",
          "SCTID:718224004",
          "UMLS:C0015458"
        ],
        "synonyms": [
          "Romberg syndrome",
          "hemifacial atrophy",
          "parry-Romberg syndrome",
          "progressive facial hemiatrophy",
          "progressive hemifacial atrophy",
          "HFA",
          "PHA",
          "Romberg hemi-facial atrophy",
          "hemifacial atrophy, progressive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Progressive hemifacial atrophy (PHA) is a rare acquired disorder, characterized by unilateral slowly progressive atrophy of the skin and soft tissues of half of the face leading to a sunken appearance. Muscles, cartilage and the underlying bony structures may also be involved."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007710"
    },
    {
      "id": 9067,
      "label": "clonic hemifacial spasm",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        7073
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017137",
          "ICD10CM:G51.3",
          "MEDGEN:374760",
          "MESH:C564198",
          "OMIM:141405",
          "Orphanet:221083",
          "UMLS:C1841639",
          "icd11.foundation:353312397",
          "icd11.foundation:64352031"
        ],
        "synonyms": [
          "facial hemispasm",
          "focal myoclonus of face",
          "hemifacial spasm",
          "hemifacial spasm, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007713"
    },
    {
      "id": 9297,
      "label": "Melkersson-Rosenthal syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        4239,
        4370,
        7148
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1761",
          "EFO:1001039",
          "GARD:0007010",
          "ICD10CM:G51.2",
          "MEDGEN:6291",
          "MESH:D008556",
          "MedDRA:10027166",
          "NCIT:C84886",
          "NORD:1429",
          "OMIM:155900",
          "Orphanet:2483",
          "UMLS:C0025235"
        ],
        "synonyms": [
          "Melkersson's syndrome",
          "Melkersson-Rosenthal syndrome",
          "MRS",
          "Melkersson syndrome",
          "Mros",
          "cheilitis Granulomatosa"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "The Melkersson-Rosenthal syndrome is a rare disorder characterized by a triad of recurrent orofacial swelling, relapsing facial paralysis and fissured tongue and onset in childhood or early adolescence. It has an estimated incidence of 8/10,000. The etiology is unknown but hereditary predisposition is suspected."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007969"
    },
    {
      "id": 9332,
      "label": "Mobius syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4235,
        4370,
        4427,
        16052,
        16088
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13501",
          "GARD:0008549",
          "ICD9:759.89",
          "MEDGEN:66357",
          "MESH:D020331",
          "MedDRA:10027789",
          "MedDRA:10030069",
          "NANDO:1200559",
          "NANDO:2200980",
          "NCIT:C84893",
          "NORD:1453",
          "OMIM:157900",
          "Orphanet:570",
          "SCTID:89444000",
          "UMLS:C0221060"
        ],
        "synonyms": [
          "MBS",
          "Mobius syndrome",
          "Moebius Syndrome",
          "Moebius sequence",
          "Moebius syndrome",
          "Moebius syndrome, Isolated cases",
          "Möbius syndrome",
          "congenital facial diplegia",
          "oromandibular-limb hypogenesis spectrum",
          "absence or underdevelopment of the 6th and 7th cranial nerves",
          "congenital facial diplegia syndrome",
          "congenital oculofacial paralysis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Moebius syndrome is a very rare congenital cranial dysinnervation disorder characterized by complete or incomplete facial paralysis in association with bilateral palsy of the abducens nerve causing impairment of ocular abduction. The syndrome also includes various other congenital anomalies."
      },
      "child_count": 5,
      "reference_id": "MONDO:0008006"
    },
    {
      "id": 16905,
      "label": "isolated facial myokymia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4235,
        7073
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:G51.4",
          "MEDGEN:78741",
          "Orphanet:221106",
          "UMLS:C0270871"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A condition that consists of spontaneous, gentle, constant, rippling contractions that spread through the affected striated muscle."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016373"
    }
  ],
  "roots": [
    {
      "id": 5469,
      "label": "cranial nerve neuropathy"
    },
    {
      "id": 5512,
      "label": "peripheral nervous system disorder"
    }
  ]
}