{
  "id": 4593,
  "label": "cutaneous mucinosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002523",
  "properties": {
    "xrefs": [
      "DOID:3141",
      "ICD9:701.8",
      "MEDGEN:56520",
      "MESH:D017520",
      "SCTID:402721001",
      "UMLS:C0162855",
      "icd11.foundation:2018255084"
    ],
    "synonyms": [
      "mucinosis",
      "mucinosis affecting the skin",
      "mucinoses"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "The mucinoses are a diverse group of disorders which have in common the deposition of basophilic, finely granular and stringy material (mucin) in the connective tissues of the dermis (dermal mucinoses), in the pilosebaceous follicles (follicular mucinoses), or in the epidermis and tumors derived therefrom (epithelial mucinoses)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 6820,
      "label": "skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4198
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:37",
          "EFO:0000701",
          "ICD9:702",
          "ICD9:702.8",
          "ICD9:709.8",
          "MEDGEN:20777",
          "MESH:D012871",
          "NANDO:2100281",
          "NCIT:C3371",
          "SCTID:95320005",
          "UMLS:C0037274"
        ],
        "synonyms": [
          "cutaneous disorder",
          "disease of zone of skin",
          "disease or disorder of zone of skin",
          "disorder of skin",
          "disorder of zone of skin",
          "skin diseases and manifestations",
          "skin disorder",
          "zone of skin disease",
          "zone of skin disease or disorder",
          "dermatosis",
          "genodermatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005093"
    }
  ],
  "children": [
    {
      "id": 8081,
      "label": "scleredema adultorum",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4593
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3140",
          "EFO:1000762",
          "GARD:0005975",
          "MEDGEN:11346",
          "MESH:D012592",
          "NCIT:C85057",
          "Orphanet:352763",
          "SCTID:95323007",
          "UMLS:C0036413"
        ],
        "synonyms": [
          "Buschke scleredema",
          "Buschke's scleredema",
          "Buschkes scleredema",
          "Diabeticorum, scleredema",
          "Diabeticorums, scleredema",
          "scleredema",
          "scleredema Diabeticorum",
          "scleredema Diabeticorum of Buschke",
          "scleredema Diabeticorums",
          "scleredema adultorum",
          "scleredema adultorum of Buschke",
          "scleredema, Buschke's",
          "scleredemas",
          "Buschke scleredema Diabeticorum",
          "Buschke scleredema adultorum"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A usually benign and self-limited skin disorder of unknown etiology, characterized by induration of the skin. It may be associated with infection, diabetes mellitus, and hematologic malignancies. Morphologically, there is deposition of mucin in the dermis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0006606"
    },
    {
      "id": 18480,
      "label": "lichen myxedematosus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4593,
        20387
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021709",
          "ICD9:701.8",
          "MEDGEN:1848864",
          "Orphanet:402007",
          "SCTID:111197009",
          "UMLS:C5848049"
        ],
        "synonyms": [
          "lichen myxoedematosus",
          "lichenoid myxedema",
          "papular mucinosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0018432"
    },
    {
      "id": 20705,
      "label": "cutaneous focal mucinosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4593
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:701.8",
          "MEDGEN:590585",
          "SCTID:110981005",
          "UMLS:C0406659"
        ],
        "synonyms": [
          "focal mucinoses",
          "focal mucinosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0021653"
    },
    {
      "id": 20706,
      "label": "diffuse cutaneous mucinosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4593
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:701.8",
          "MEDGEN:590581",
          "SCTID:238945000",
          "UMLS:C0406655"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0021654"
    },
    {
      "id": 20707,
      "label": "secondary catabolic mucinosis of skin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4593
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:701.8",
          "MEDGEN:697525",
          "SCTID:402723003",
          "UMLS:C1274173"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0021655"
    }
  ],
  "roots": [
    {
      "id": 6820,
      "label": "skin disorder"
    }
  ]
}