{
  "id": 14042,
  "label": "isolated congenital hypoglossia/aglossia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013003",
  "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)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3409,
      "label": "tongue disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10944",
          "ICD9:529.8",
          "ICD9:529.9",
          "MEDGEN:52777",
          "MESH:D014060",
          "NCIT:C173793",
          "SCTID:69244009",
          "UMLS:C0040409",
          "icd11.foundation:928435705"
        ],
        "synonyms": [
          "disease of tongue",
          "disease or disorder of tongue",
          "disorder of tongue",
          "tongue disease",
          "tongue disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A disease involving the tongue."
      },
      "child_count": 9,
      "reference_id": "MONDO:0001165"
    },
    {
      "id": 17499,
      "label": "oromandibular-limb hypogenesis syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16328
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004116",
          "MEDGEN:1843329",
          "Orphanet:2749",
          "UMLS:C5679764",
          "icd11.foundation:1665391511"
        ],
        "synonyms": [
          "Oroacral syndrome",
          "oro-mandibular-limb hypogenesis syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Oromandibular-limb hypogenesis syndromes (OLHS) are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) characterized by the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies)."
      },
      "child_count": 8,
      "reference_id": "MONDO:0017139"
    }
  ],
  "children": [
    {
      "id": 22841,
      "label": "isolated congenital aglossia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        14042
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035410"
    },
    {
      "id": 22842,
      "label": "isolated congenital hypoglossia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        14042
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022264",
          "ICD10CM:Q38.3",
          "MEDGEN:10029",
          "Orphanet:563954",
          "UMLS:C0025988"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0035411"
    }
  ],
  "roots": [
    {
      "id": 3409,
      "label": "tongue disorder"
    },
    {
      "id": 17499,
      "label": "oromandibular-limb hypogenesis syndrome"
    }
  ]
}