{
  "id": 12216,
  "label": "isolated hereditary congenital facial paralysis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011090",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 21422,
      "label": "facial paresis, hereditary congenital, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        12216
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024466"
    }
  ],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}