{
  "id": 19272,
  "label": "localized lichen myxedematosus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019446",
  "properties": {
    "xrefs": [
      "GARD:0007321",
      "MEDGEN:1802421",
      "Orphanet:86795",
      "UMLS:C5575846",
      "icd11.foundation:15830032"
    ],
    "synonyms": [
      "papular mucinosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Localized lichen myxedematosus is a group of skin diseases characterized by the development of papules, nodules and/or plaques with mucin deposits and a variable degree of fibrosis in the absence of thyroid disease. The group comprises five sub-forms: nodular lichen myxedematosus, discrete papular lichen myxedematosus, papular mucinosis of infancy, acral persistent papular mucinosis and self-healing papular mucinosis."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 19383,
      "label": "nodular lichen myxedematosus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019137",
          "MEDGEN:894327",
          "Orphanet:90393",
          "SCTID:717257000",
          "UMLS:C4273968"
        ],
        "synonyms": [
          "atypical tuberous myxedema of Jadassohn-Dosseker"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Nodular lichen myxedematosus is a rare form of localized lichen myxedematosus characterized by the development of skin-coloured mucinous nodules on the limbs and trunk, with mild or absent papular eruption."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019578"
    },
    {
      "id": 19384,
      "label": "discrete papular lichen myxedematosus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019138",
          "MEDGEN:898313",
          "Orphanet:90394",
          "SCTID:717258005",
          "UMLS:C4273967"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Discrete papular lichen myxedematosus is a rare chronic, slowly progressive form of localized lichen myxedematosus characterized by the development of a few to multiple small symmetrical skin-coloured mucinous papules on the limbs and trunk."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019579"
    },
    {
      "id": 19385,
      "label": "papular mucinosis of infancy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019139",
          "MEDGEN:909529",
          "Orphanet:90395",
          "SCTID:717259002",
          "UMLS:C4273966"
        ],
        "synonyms": [
          "cutaneous mucinosis of infancy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Papular mucinosis of infancy is a rare pediatric non progressive form of localized lichen myxedematosus characterized by the development of firm opalescent mucinous papules on the upper arms and the trunk."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019580"
    },
    {
      "id": 19386,
      "label": "acral persistent papular mucinosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019140",
          "ICD9:701.8",
          "MEDGEN:590586",
          "Orphanet:90396",
          "SCTID:238949006",
          "UMLS:C0406660",
          "icd11.foundation:712202928"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Acral persistent papular mucinosis is a rare chronic form of localized lichen myxedematosus characterized by the development of multiple symmetrical skin-colored mucinous papules exclusively on the extensor surface of the hands and distal forearms."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019581"
    },
    {
      "id": 19387,
      "label": "self-healing papular mucinosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019141",
          "MEDGEN:590583",
          "Orphanet:90397",
          "UMLS:C0406657"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Self-healing papular mucinosis is a rare form of localized lichen myxedematosus occurring primarily in children and characterized by the development of mucinous papules on various parts of the body (face, neck, trunk, and limbs) that resolve spontaneously within some weeks to months. Systemic symptoms can be observed such as fever, arthralgias and weakness."
      },
      "child_count": 0,
      "reference_id": "MONDO:0019582"
    }
  ],
  "roots": [
    {
      "id": 18480,
      "label": "lichen myxedematosus"
    }
  ]
}