{
  "id": 20278,
  "label": "hereditary sebaceous gland anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021029",
  "properties": {
    "xrefs": [
      "GARD:0020268",
      "MEDGEN:1843175",
      "Orphanet:183460",
      "UMLS:C5680577"
    ],
    "synonyms": [
      "genetic sebaceous gland anomaly"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "An instance of sebaceous gland anomaly that is caused by a modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20277,
      "label": "hereditary epidermal appendage anomaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020265",
          "MEDGEN:1843118",
          "Orphanet:183447",
          "UMLS:C5680583"
        ],
        "synonyms": [
          "genetic epidermal appendage anomaly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of epidermal appendage anomaly that is caused by a modification of the individual's genome."
      },
      "child_count": 3,
      "reference_id": "MONDO:0021026"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20277,
      "label": "hereditary epidermal appendage anomaly"
    }
  ]
}