{
  "id": 22841,
  "label": "isolated congenital aglossia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0035410",
  "properties": {
    "xrefs": [
      "GARD:0022263",
      "ICD10CM:Q38.3",
      "MEDGEN:57859",
      "Orphanet:563951",
      "UMLS:C0158663"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 14042,
      "label": "isolated congenital hypoglossia/aglossia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3409,
        17499
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016972",
          "MEDGEN:411249",
          "OMIM:612776",
          "Orphanet:141152",
          "UMLS:C2748587"
        ],
        "synonyms": [
          "hypoglossia with situs inversus",
          "hypoglossia, isolated"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Isolated aglossia and hypoglossia are terms covering the spectrum from partial to total absence of the tongue. These congenital malformations have been classified as part of the group of oromandibular-limb hypogenesis syndromes (OLHS)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0013003"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 14042,
      "label": "isolated congenital hypoglossia/aglossia"
    }
  ]
}