{
  "id": 21422,
  "label": "facial paresis, hereditary congenital, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024466",
  "properties": {
    "xrefs": [
      "GARD:0025400",
      "MEDGEN:371292",
      "OMIM:601471",
      "UMLS:C1832284"
    ],
    "synonyms": [
      "HCFP1",
      "facial paresis, hereditary congenital, 1",
      "Mobius syndrome 2",
      "Mobius syndrome 2, formerly",
      "Moebius syndrome 2",
      "Moebius syndrome 2, formerly",
      "facial palsy, congenital, unilateral or bilateral"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12216,
      "label": "isolated hereditary congenital facial paralysis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008583",
          "MEDGEN:1381843",
          "MESH:C563309",
          "OMIMPS:601471",
          "Orphanet:306527",
          "SCTID:733091002",
          "UMLS:C4518577"
        ],
        "synonyms": [
          "HCFP",
          "MBS2 (formerly)",
          "Mobius syndrome 2 (formerly)",
          "Moebius syndrome 2 (formerly)",
          "facial palsy, congenital, unilateral or bilateral",
          "facial paresis hereditary congenital",
          "facial paresis, hereditary congenital",
          "hereditary congenital facial paresis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal."
      },
      "child_count": 2,
      "reference_id": "MONDO:0011090"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 12216,
      "label": "isolated hereditary congenital facial paralysis"
    }
  ]
}