{
  "id": 22384,
  "label": "amelogenesis imperfecta, type 3C",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032717",
  "properties": {
    "xrefs": [
      "DOID:0111722",
      "GARD:0025728",
      "MEDGEN:1676410",
      "OMIM:618386",
      "UMLS:C5193069"
    ],
    "synonyms": [
      "AI3C",
      "AMELOGENESIS IMPERFECTA, TYPE IIIC",
      "Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0006858",
        "name": "mouth disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25961,
      "label": "hypocalcified amelogenesis imperfecta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19324
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016931",
          "MEDGEN:140773",
          "Orphanet:100032",
          "UMLS:C0399376",
          "icd11.foundation:1793262466"
        ],
        "synonyms": [
          "amelogenesis imperfecta type 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0006858",
            "name": "mouth disorder"
          }
        ]
      },
      "child_count": 3,
      "reference_id": "MONDO:0968955"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25961,
      "label": "hypocalcified amelogenesis imperfecta"
    }
  ]
}