{
  "id": 11783,
  "label": "keratosis follicularis spinulosa decalvans, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010637",
  "properties": {
    "xrefs": [
      "DOID:0080754",
      "GARD:0015299",
      "MEDGEN:854384",
      "MESH:C536159",
      "OMIM:308800",
      "UMLS:C3887525"
    ],
    "synonyms": [
      "keratosis follicularis spinulosa decalvans, X-linked",
      "keratosis follicularis spinulosa decalvans, X-linked, X-linked recessive",
      "KFSDX",
      "Kfsdx",
      "keratosis follicularis SPINULOSA decalvans, X-linked",
      "keratosis follicularis Spinulosa decalvans cum Ophiasi",
      "keratosis follicularis spinulosa decalvans",
      "keratosis follicularis spinulosa decalvans cum ophiasi"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2737,
      "label": "keratosis follicularis spinulosa decalvans",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8047,
        18791,
        24863
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080753",
          "GARD:0006829",
          "ICD9:757.39",
          "MEDGEN:83355",
          "NORD:1288",
          "Orphanet:2340",
          "SCTID:238626006",
          "UMLS:C0343057",
          "icd11.foundation:303213910"
        ],
        "synonyms": [
          "keratosis pilaris decalvans"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Keratosis follicularis spinulosa decalvans is a rare genodermatosis occurring during infancy or childhood, predominantly affecting males, and characterized by diffuse follicular hyperkeratosis associated with progressive cicatricial alopecia of the scalp, eyebrows and eyelashes. Additional findings can include photophobia, corneal dystrophy, facial erythema, and/or palmoplantar keratoderma."
      },
      "child_count": 6,
      "reference_id": "MONDO:0000136"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2737,
      "label": "keratosis follicularis spinulosa decalvans"
    }
  ]
}