{
  "id": 10042,
  "label": "amelogenesis imperfecta type 1C",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008770",
  "properties": {
    "xrefs": [
      "DOID:0110056",
      "GARD:0015136",
      "MEDGEN:388763",
      "MESH:C567147",
      "OMIM:204650",
      "UMLS:C2673923"
    ],
    "synonyms": [
      "AI1C",
      "amelogenesis imperfecta, type 1C",
      "amelogenesis imperfecta, hypoplastic, with or without Openbite malocclusion, autosomal recessive",
      "amelogenesis imperfecta, local hypoplastic type, autosomal recessive",
      "amelogenesis imperfecta, type IC"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16023,
      "label": "amelogenesis imperfecta type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000645",
          "ICD9:520.5",
          "MEDGEN:97992",
          "Orphanet:100031",
          "SCTID:109476006",
          "UMLS:C0399367"
        ],
        "synonyms": [
          "hypoplastic amelogenesis imperfecta"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0015047"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16023,
      "label": "amelogenesis imperfecta type 1"
    }
  ]
}