{
  "id": 9217,
  "label": "tooth agenesis, selective, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007881",
  "properties": {
    "xrefs": [
      "GARD:0018245",
      "MEDGEN:372057",
      "MESH:C563634",
      "OMIM:150400",
      "UMLS:C1835492"
    ],
    "synonyms": [
      "WNT10A tooth agenesis",
      "tooth agenesis caused by mutation in WNT10A",
      "tooth agenesis, selective, 4",
      "tooth agenesis, selective, type 4",
      "STHAG4",
      "lateral incisors, absence of",
      "lateral incisors, pegged or missing",
      "succedaneous teeth, agenesis of",
      "tooth agenesis, selective, 4, with or without ectodermal dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Any tooth agenesis in which the cause of the disease is a mutation in the WNT10A gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7142,
      "label": "tooth agenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        8422
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050591",
          "EFO:0005410",
          "ICD10CM:K00.0",
          "ICD9:520.0",
          "MEDGEN:43794",
          "OMIMPS:106600",
          "Orphanet:2227",
          "Orphanet:99798",
          "SCTID:64969001",
          "UMLS:C0020608",
          "icd11.foundation:1559717619"
        ],
        "synonyms": [
          "hypodontia",
          "selective tooth agenesis",
          "tooth agenesis, selective",
          "oligodontia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "A tooth disease characterized by failure to develop one or more missing teeth."
      },
      "child_count": 24,
      "reference_id": "MONDO:0005486"
    },
    {
      "id": 24086,
      "label": "ectodermal dysplasia WNT10A related",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19138
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026153"
        ],
        "synonyms": [
          "ectodermal dysplasia WNT10A related"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0100358"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7142,
      "label": "tooth agenesis"
    },
    {
      "id": 24086,
      "label": "ectodermal dysplasia WNT10A related"
    }
  ]
}