{
  "id": 24715,
  "label": "monilethrix-2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700341",
  "properties": {
    "xrefs": [
      "DOID:0061152",
      "GARD:0028015",
      "MEDGEN:1876490",
      "OMIM:621169",
      "UMLS:C6012713"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9335,
      "label": "monilethrix",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050472",
          "GARD:0000093",
          "MEDGEN:108185",
          "MESH:D056734",
          "NCIT:C84894",
          "NORD:1454",
          "OMIMPS:158000",
          "Orphanet:573",
          "SCTID:69488000",
          "UMLS:C0546966",
          "icd11.foundation:415074833"
        ],
        "synonyms": [
          "monilethrix",
          "moniliform hair syndrome",
          "MNLIX",
          "nodose hair"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Monilethrix is a rare genodermatosis characterized by a hair shaft dysplasia resulting in hypotrichosis."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008009"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9335,
      "label": "monilethrix"
    }
  ]
}