{
  "id": 18791,
  "label": "keratosis pilaris atrophicans",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018855",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 19129,
      "label": "epidermal disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842776",
          "Orphanet:79353",
          "UMLS:C5681492"
        ],
        "synonyms": [
          "epidermal disease",
          "rare epidermal disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A skin disease that involves the epidermis."
      },
      "child_count": 25,
      "reference_id": "MONDO:0019268"
    },
    {
      "id": 20282,
      "label": "keratosis pilaris",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:82664",
          "NCIT:C124070",
          "SCTID:5132005",
          "UMLS:C0263383",
          "icd11.foundation:1614890502"
        ],
        "synonyms": [
          "KP"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A form of dry skin characterized by hair follicles plugged by scale."
      },
      "child_count": 1,
      "reference_id": "MONDO:0021036"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "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"
    },
    {
      "id": 10116,
      "label": "atrophoderma vermiculata",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18791
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008849"
    },
    {
      "id": 18246,
      "label": "ulerythema ophryogenesis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18791
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0005395",
          "MEDGEN:1813086",
          "Orphanet:3406",
          "UMLS:C5700076"
        ],
        "synonyms": [
          "keratosis pilaris affecting the follicles of the eyebrow hairs",
          "type of genodermatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Ulerythema ophryogenesis is characterized by inflammatory keratotic papules occurring on the face, which may be followed by scars, atrophy and alopecia. Prevalence is unknown but the disease, affecting mainly children and young adults, is rare. Erythema with mild hyperkeratosis of the hair follicles resulting in rough papules is observed on the cheeks and lateral aspects of the eyebrows. The disorder occasionally extends to the adjacent scalp, ears and forehead and rarely to the extensor surfaces of the limbs. Symptoms regress with age, although loss of the lateral aspects of the eyebrows can occur. Many cases occur sporadically; autosomal dominant inheritance has also been reported. There is no particular treatment, but patients should avoid sun exposure without UV protection."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018086"
    },
    {
      "id": 25547,
      "label": "keratosis pilaris atrophicans faciei",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18791
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080752",
          "GARD:0026752"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A keratosis pilaris atrophicans that is characterized by scar-like follicular depressions and loss of hair primarily in the eyebrow area."
      },
      "child_count": 0,
      "reference_id": "MONDO:0859588"
    }
  ],
  "roots": [
    {
      "id": 19129,
      "label": "epidermal disease"
    },
    {
      "id": 20282,
      "label": "keratosis pilaris"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}