{
  "id": 23507,
  "label": "keratinization disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0045011",
  "properties": {
    "xrefs": [
      "MEDGEN:635020",
      "SCTID:277905003",
      "UMLS:C0475811"
    ],
    "synonyms": [
      "disorder of keratinization",
      "keratinization disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4198,
      "label": "integumentary system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:16",
          "EFO:0010285",
          "MEDGEN:712400",
          "SCTID:128598002",
          "UMLS:C1290011"
        ],
        "synonyms": [
          "disease of integumental system",
          "disease or disorder of integumental system",
          "disorder of integumental system",
          "integumental system disease",
          "integumental system disease or disorder",
          "integumentary disease",
          "disorder of integument"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease involving the integumental system."
      },
      "child_count": 36,
      "reference_id": "MONDO:0002051"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [
    {
      "id": 8047,
      "label": "keratosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820,
        23507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:161",
          "EFO:1000720",
          "MEDGEN:9625",
          "MESH:D007642",
          "NCIT:C34745",
          "SCTID:254666005",
          "UMLS:C0022593"
        ],
        "synonyms": [
          "keratoderma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A skin disorder consisting of hypertrophy of the stratum corneum of the skin."
      },
      "child_count": 18,
      "reference_id": "MONDO:0006566"
    },
    {
      "id": 8644,
      "label": "epidermolytic ichthyosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17595,
        23507
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4603",
          "GARD:0024537",
          "MEDGEN:38179",
          "MESH:D017488",
          "NORD:1100",
          "OMIMPS:113800",
          "SCTID:254167000",
          "UMLS:C0079153",
          "icd11.foundation:1183730789"
        ],
        "synonyms": [
          "BCIE",
          "EHK",
          "EI",
          "bullous congenital ichthyosiform erythroderma",
          "bullous congenital ichthyosiform erythroderma of Brock",
          "bullous ichthyosis",
          "epidermolytic hyperkeratosis",
          "epidermolytic ichthyosis",
          "ichthyosis hystrix Brocq type",
          "autosomal dominant epidermolytic ichthyosis",
          "bullous erythroderma Ichthyosiformis congenita of Brocq",
          "bullous ichthyosiform erythroderma",
          "bullous ichthyosiform erythroderma congenita",
          "congenital bullous ichthyosiform erythroderma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A rare keratinopathic ichthyosis (KPI), that is characterized by a blistering phenotype at birth which progressively becomes hyperkeratotic."
      },
      "child_count": 8,
      "reference_id": "MONDO:0007239"
    }
  ],
  "roots": [
    {
      "id": 4198,
      "label": "integumentary system disorder"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}