{
  "id": 10116,
  "label": "atrophoderma vermiculata",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008849",
  "properties": {
    "xrefs": [
      "DOID:0080756",
      "GARD:0009744",
      "ICD9:701.8",
      "MEDGEN:82666",
      "OMIM:209700",
      "Orphanet:79100",
      "SCTID:2736005",
      "UMLS:C0263429"
    ],
    "synonyms": [
      "atrophoderma vermiculata",
      "folliculitis ulerythematosa reticulate",
      "Atrophodermia reticulata",
      "Atrophodermia reticulata symmetrica faciei",
      "Atrophodermia vermiculata",
      "atrophoderma vermiculatum",
      "ava",
      "folliculitis ulerythematosa",
      "folliculitis ulerythematosa reticulata",
      "honeycomb atrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18791,
      "label": "keratosis pilaris atrophicans",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19129,
        20282,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080751",
          "GARD:0018694",
          "ICD9:757.39",
          "MEDGEN:75520",
          "MESH:C537412",
          "OMIM:604093",
          "Orphanet:498",
          "SCTID:400059005",
          "UMLS:C0263428",
          "icd11.foundation:273325594"
        ],
        "synonyms": [
          "keratosis pilaris atrophicans",
          "Atrophodermia reticulata",
          "Atrophodermia reticulata symmetrica faciei",
          "Atrophodermia vermiculata",
          "KPA",
          "amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2",
          "burnett Schwartz Berberian syndrome",
          "folliculitis ulerythematosa",
          "folliculitis ulerythematosa reticulata",
          "honeycomb atrophy",
          "keratosis pilaris",
          "keratosis pilaris atrophicans facies",
          "ulerythema ophryogenes",
          "ulerythema ophryogenes with multiple congenital anomalies",
          "ulerythema ophryogenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An uncommon form of keratosis pilaris in which there are scar-like follicular depressions and loss of hair."
      },
      "child_count": 12,
      "reference_id": "MONDO:0018855"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18791,
      "label": "keratosis pilaris atrophicans"
    }
  ]
}