{
  "id": 23445,
  "label": "large congenital melanocytic nevus",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0044792",
  "properties": {
    "xrefs": [
      "DOID:0111359",
      "GARD:0002469",
      "ICDO:8761/1",
      "MEDGEN:330752",
      "MedDRA:10072036",
      "NCIT:C3944",
      "NCIT:C4234",
      "NORD:1184",
      "OMIM:137550",
      "ONCOTREE:SKCN",
      "Orphanet:626",
      "SCTID:254815002",
      "SCTID:398696001",
      "UMLS:C1842036",
      "icd11.foundation:618273329"
    ],
    "synonyms": [
      "Giant Congenital Melanocytic Nevus",
      "bathing trunk nevus",
      "congenital melanocytic nevi",
      "congenital melanocytic nevus",
      "congenital melanocytic nevus of skin",
      "congenital melanocytic nevus of the skin",
      "congenital nevus of skin",
      "congenital nevus of the skin",
      "congenital pigmented melanocytic Nevus",
      "congenital pigmented nevus of skin",
      "congenital pigmented nevus of the skin",
      "congenital pigmented skin nevus",
      "congenital skin nevus",
      "giant congenital nevus",
      "giant pigmented hairy nevus",
      "giant pigmented nevus of skin",
      "giant pigmented nevus of the skin",
      "large congenital melanocytic nevus",
      "melanocytic nevus syndrome, congenital, somatic",
      "spitz nevus or nevus spilus, somatic",
      "CMNS",
      "GPHN",
      "congenital giant pigmented nevus",
      "congenital hairy nevus",
      "congenital nevus",
      "giant congenital melanocytic nevus",
      "giant congenital pigmented Nevus",
      "giant hairy nevus",
      "giant pigmented nevus",
      "melanocytic nevus syndrome, congenital",
      "nevus spilus",
      "pigmented moles",
      "spitz nevus"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A large, or giant, congenital melanocytic nevus (LCMN or GCMN) is a pigmented skin lesion of more than 20 cm - or 40 cm- respectively, projected adult diameter, composed of melanocytes, and presenting with an elevated risk of malignant transformation."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6801,
      "label": "melanocytic nevus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20564,
        20680
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0009675",
          "MEDGEN:14364",
          "MESH:D009506",
          "NCIT:C7570",
          "SCTID:400096001",
          "UMLS:C0027962",
          "Wikipedia:Nevus"
        ],
        "synonyms": [
          "melanocytic Nevus",
          "melanotic Nevus",
          "mole",
          "mole of skin",
          "nevus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A neoplasm composed of melanocytes that usually appears as a dark spot on the skin."
      },
      "child_count": 56,
      "reference_id": "MONDO:0005073"
    },
    {
      "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": 6801,
      "label": "melanocytic nevus"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}