{
  "id": 5879,
  "label": "dental enamel hypoplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004038",
  "properties": {
    "xrefs": [
      "DOID:693",
      "EFO:1001304",
      "MEDGEN:3730",
      "MESH:D003744",
      "NCIT:C34529",
      "SCTID:26597004",
      "UMLS:C0011351"
    ],
    "synonyms": [
      "enamel hypoplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ],
    "definition": "Deficiency in the enamel tissue that results in the formation of grooves, pits, or dents on the surface of the affected teeth."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4339,
      "label": "tooth hard tissue disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8422
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:214",
          "ICD10CM:K03",
          "ICD9:521.8",
          "ICD9:521.89",
          "MEDGEN:510140",
          "SCTID:46557008",
          "UMLS:C0155926"
        ],
        "synonyms": [
          "disorder of hard tissues of teeth",
          "teeth hard tissue disease",
          "teeth hard tissue diseases"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0002220"
    }
  ],
  "children": [
    {
      "id": 19324,
      "label": "amelogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        5879
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:0828-0533",
          "DOID:2187",
          "GARD:0005791",
          "ICD9:520.5",
          "MEDGEN:240",
          "MESH:D000567",
          "NORD:765",
          "OMIMPS:104500",
          "Orphanet:88661",
          "SCTID:78494001",
          "UMLS:C0002452",
          "icd11.foundation:1923123066"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ],
        "definition": "Amelogenesis imperfecta (AI) represents a group of developmental conditions affecting the structure and clinical appearance of the enamel of all or nearly all the teeth in a more or less equal manner, and which may be associated with morphologic or biochemical changes elsewhere in the body."
      },
      "child_count": 14,
      "reference_id": "MONDO:0019507"
    }
  ],
  "roots": [
    {
      "id": 4339,
      "label": "tooth hard tissue disease"
    }
  ]
}