{
  "id": 13026,
  "label": "melanoma, cutaneous malignant, susceptibility to, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011954",
  "properties": {
    "xrefs": [
      "GARD:0027809",
      "MEDGEN:334129",
      "OMIM:608035",
      "UMLS:C1842643"
    ],
    "synonyms": [
      "CMM4",
      "melanoma, cutaneous malignant, 4",
      "melanoma, cutaneous malignant, susceptibility to, 4"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 21418,
      "label": "susceptibility to familial cutaneous melanoma"
    }
  ]
}