{
  "id": 9292,
  "label": "melanoma, cutaneous malignant, susceptibility to, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007964",
  "properties": {
    "xrefs": [
      "DOID:10041",
      "GARD:0027783",
      "MEDGEN:331891",
      "MESH:D004416",
      "NCIT:C7584",
      "OMIM:155601",
      "UMLS:C1835044"
    ],
    "synonyms": [
      "Atypical Mole syndrome",
      "B-K Mole syndrome",
      "dysplastic nevus syndrome",
      "familial dysplastic nevi",
      "melanoma, cutaneous malignant, 2",
      "melanoma, cutaneous malignant, susceptibility to, 2",
      "melanoma, cutaneous malignant, susceptibility to, type 2",
      "CMM2",
      "susceptibility to cutaneous malignant melanoma 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Clinically atypical nevi (usually exceeding 5 mm in diameter and having variable pigmentation and ill defined borders) with an increased risk for development of non-familial cutaneous malignant melanoma. Biopsies show melanocytic dysplasia. Nevi are clinically and histologically identical to the precursor lesions for melanoma in the B-K mole syndrome. (Stedman, 25th ed)"
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2903,
      "label": "autosomal dominant disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2905
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050736",
          "ICD9:758.5",
          "MEDGEN:539206",
          "SCTID:11164009",
          "UMLS:C0265385"
        ],
        "synonyms": [
          "autosomal dominant disease or disorder",
          "autosomal dominant hereditary disorder",
          "autosomal dominant inherited disorder",
          "disease or disorder, autosomal dominant",
          "disease, autosomal dominant"
        ],
        "definition": "Autosomal dominant form of disease."
      },
      "child_count": 192,
      "reference_id": "MONDO:0000426"
    },
    {
      "id": 21418,
      "label": "susceptibility to familial cutaneous melanoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027916",
          "MEDGEN:1388845",
          "OMIMPS:155600",
          "UMLS:C4511622"
        ],
        "synonyms": [
          "hereditary cutaneous melanoma (disease)",
          "melanoma, cutaneous malignant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A susceptibility or predisposition to cutaneous melanoma (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 10,
      "reference_id": "MONDO:0024462"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2903,
      "label": "autosomal dominant disease"
    },
    {
      "id": 21418,
      "label": "susceptibility to familial cutaneous melanoma"
    }
  ]
}