{
  "id": 11644,
  "label": "Olmsted syndrome, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010486",
  "properties": {
    "xrefs": [
      "DOID:0112012",
      "GARD:0015273",
      "MEDGEN:813075",
      "OMIM:300918",
      "UMLS:C3806745"
    ],
    "synonyms": [
      "Olmsted syndrome, X-linked",
      "Olmsted syndrome, X-linked, X-linked recessive",
      "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 22242,
      "label": "Olmsted syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19132
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112011",
          "GARD:0004075",
          "MEDGEN:590661",
          "MedDRA:10068842",
          "OMIMPS:614594",
          "Orphanet:659",
          "UMLS:C0406761"
        ],
        "synonyms": [
          "mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques",
          "palmoplantar and periorificial keratoderma",
          "palmoplantar keratoderma, mutilating, with periorificial keratotic plaques"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques."
      },
      "child_count": 3,
      "reference_id": "MONDO:0031421"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 22242,
      "label": "Olmsted syndrome"
    }
  ]
}