{
  "id": 10068,
  "label": "anodontia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008797",
  "properties": {
    "xrefs": [
      "DOID:13714",
      "GARD:0005818",
      "ICD9:520.0",
      "MEDGEN:98313",
      "MESH:D000848",
      "MedDRA:10002583",
      "OMIM:206780",
      "Orphanet:99797",
      "SCTID:16958000",
      "UMLS:C0399352",
      "icd11.foundation:413433873"
    ],
    "synonyms": [
      "complete absence of teeth",
      "developmental absence of tooth",
      "total anodontia of permanent and deciduous teeth",
      "absence of permanent teeth",
      "anodontia of permanent dentition",
      "teeth, permanent, absence of"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Anodontia is an extreme developmental dental anomaly characterized by the complete absence of all teeth."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 8422,
      "label": "tooth disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6893,
        8301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1091",
          "EFO:1001216",
          "MEDGEN:11852",
          "MESH:D014076",
          "NCIT:C35077",
          "SCTID:234947003",
          "UMLS:C0040435"
        ],
        "synonyms": [
          "calcareous tooth disease",
          "calcareous tooth disease or disorder",
          "dental disorder",
          "disease of calcareous tooth",
          "disease or disorder of calcareous tooth",
          "disorder of calcareous tooth",
          "tooth disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A disease involving the calcareous tooth."
      },
      "child_count": 22,
      "reference_id": "MONDO:0006999"
    }
  ],
  "children": [
    {
      "id": 20766,
      "label": "Aloi Tomasini Isaia syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        10068
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000417",
          "MEDGEN:419073",
          "MESH:C537049",
          "UMLS:C2931405"
        ],
        "synonyms": [
          "basal cell nevus anodontia abnormal bone mineralization",
          "basal cell nevus, anodontia, abnormal bone mineralization",
          "unilateral linear basal cell nevus associated with diffuse osteoma cutis, unilateral anodontia, and abnormal bone mineralization"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A syndrome characterized by a unilateral linear basal cell nevus, diffuse osteoma cutis, unilateral anodontia (missing teeth), and abnormal bone mineralization. This is an n-of-1 use case where only one patient or family has been described with this disorder."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021845"
    },
    {
      "id": 23134,
      "label": "mehta lewis patton syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3108,
        7116,
        10068,
        16310,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003450",
          "MEDGEN:419340",
          "MESH:C536147",
          "UMLS:C2931120"
        ],
        "synonyms": [
          "congenital heart disease, ptosis, hypodontia, and craniosynostosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0043127"
    },
    {
      "id": 23141,
      "label": "microdontia hypodontia short stature",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10068,
        16330
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0003638",
          "MEDGEN:419435",
          "MESH:C537553",
          "UMLS:C2931532"
        ],
        "synonyms": [
          "microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0043141"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 8422,
      "label": "tooth disorder"
    }
  ]
}