{
  "id": 12512,
  "label": "facial paresis, hereditary congenital, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011407",
  "properties": {
    "xrefs": [
      "GARD:0018436",
      "MEDGEN:346971",
      "OMIM:604185",
      "UMLS:C1858717"
    ],
    "synonyms": [
      "facial paresis, hereditary congenital, 2",
      "HCFP2",
      "Mobius syndrome 3",
      "Mobius syndrome 3, formerly",
      "Moebius syndrome 3",
      "Moebius syndrome 3, formerly"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17904,
      "label": "congenital hereditary facial paralysis-variable hearing loss syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        21213
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017379",
          "MEDGEN:928261",
          "Orphanet:306530",
          "SCTID:722389002",
          "UMLS:C4302592"
        ],
        "synonyms": [
          "congenital hereditary facial palsy with variable deafness",
          "congenital hereditary facial palsy with variable hearing loss",
          "congenital hereditary facial paralysis with variable deafness",
          "congenital hereditary facial paralysis-variable deafness syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Congenital hereditary facial paralysis-variable hearing loss syndrome is an extremely rare autosomal recessive disorder characterized by bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears), and strabismus."
      },
      "child_count": 4,
      "reference_id": "MONDO:0017627"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17904,
      "label": "congenital hereditary facial paralysis-variable hearing loss syndrome"
    }
  ]
}