{
  "id": 8945,
  "label": "multiple self-healing squamous epithelioma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007566",
  "properties": {
    "xrefs": [
      "DOID:5585",
      "GARD:0003090",
      "MEDGEN:154270",
      "MESH:C536150",
      "NCIT:C4461",
      "OMIM:132800",
      "Orphanet:65748",
      "SCTID:254659009",
      "UMLS:C0546476"
    ],
    "synonyms": [
      "Ferguson-Smith disease",
      "Ferguson-Smith syndrome",
      "Ferguson-Smith tumor",
      "Ferguson-Smith tumour",
      "MSSE",
      "familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type",
      "multiple keratoacanthoma, Ferguson-Smith type",
      "multiple self healing epithelioma of Ferguson-Smith",
      "multiple self-healing squamous epithelioma",
      "self-healing squamous epithelioma type 1",
      "ESS1",
      "ESS1 (formerly)",
      "ESS1, formerly",
      "Ferguson-Smith type epithelioma",
      "Ferguson-Smith-type epithelioma",
      "multiple self healing squamous epithelioma",
      "multiple self-healing squamous epithelioma, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Multiple self-healing squamous epithelioma (also known as Ferguson-Smith disease (FSD)) is a rare inherited skin cancer syndrome characterized by the development of multiple locally invasive skin tumors resembling keratoacanthomas of the face and limbs which usually heal spontaneously after several months leaving pitted scars."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        20011,
        20301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019921",
          "MEDGEN:14326",
          "MESH:D009386",
          "NCIT:C3266",
          "Orphanet:140162",
          "SCTID:699346009",
          "UMLS:C0027672"
        ],
        "synonyms": [
          "cancer syndrome, hereditary",
          "cancer syndromes, hereditary",
          "familial neoplastic syndrome",
          "familial tumor syndrome",
          "familial tumour syndrome",
          "hereditary cancer syndrome",
          "hereditary cancer syndromes",
          "hereditary neoplastic syndrome",
          "hereditary neoplastic syndromes",
          "hereditary tumor syndrome",
          "hereditary tumour syndrome",
          "inherited cancer syndrome",
          "inherited cancer-predisposing syndrome",
          "neoplastic syndrome, hereditary",
          "syndrome, hereditary cancer",
          "syndrome, hereditary neoplastic",
          "syndromes, hereditary cancer",
          "syndromes, hereditary neoplastic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "The inherited predisposition toward getting a tumor."
      },
      "child_count": 351,
      "reference_id": "MONDO:0015356"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16218,
      "label": "hereditary neoplastic syndrome"
    }
  ]
}