{
  "id": 15746,
  "label": "skin creases, congenital symmetric circumferential, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014755",
  "properties": {
    "xrefs": [
      "DOID:0112243",
      "GARD:0016156",
      "MEDGEN:902880",
      "OMIM:616734",
      "UMLS:C4225225"
    ],
    "synonyms": [
      "CSCSC2",
      "MAPRE2 multiple benign circumferential skin creases on limbs",
      "multiple benign circumferential skin creases on limbs caused by mutation in MAPRE2",
      "skin creases, congenital symmetric circumferential, 2",
      "skin creases, congenital symmetric circumferential, 2; CSCSC2",
      "skin creases, congenital symmetric circumferential, type 2",
      "symmetric circumferential skin creases, congenital, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9316,
      "label": "multiple benign circumferential skin creases on limbs",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112241",
          "GARD:0003589",
          "MEDGEN:96881",
          "MESH:C537575",
          "Orphanet:2505",
          "UMLS:C0473586"
        ],
        "synonyms": [
          "CCSF",
          "CSCSC",
          "Kunze-Riehm syndrome",
          "circumferential skin creases, Kunze type",
          "congenital circumferential skin folds",
          "Kunze Riehm syndrome",
          "Michelin tire baby syndrome",
          "Michelin tyre baby syndrome",
          "skin creases, multiple benign ring-shaped, of limbs"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0007990"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 9316,
      "label": "multiple benign circumferential skin creases on limbs"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}