{
  "id": 9226,
  "label": "familial generalized lentiginosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007891",
  "properties": {
    "xrefs": [
      "GARD:0017158",
      "MEDGEN:486897",
      "MESH:C573023",
      "OMIM:151001",
      "Orphanet:231040",
      "SCTID:765195000",
      "UMLS:C3492944"
    ],
    "synonyms": [
      "familial lentigines profusa",
      "familial multiple lentigines syndrome without systemic involvement",
      "lentiginosis profusa",
      "lentiginosis, diffuse",
      "lentiginosis, generalised",
      "lentiginosis, generalized",
      "lentiginosis, inherited patterned"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Familial generalized lentiginosis is a rare, inherited, skin hyperpigmentation disorder characterized by widespread lentigines without associated noncutaneous abnormalities. Patients present multiple brown to dark brown, non-elevated macula of 0.2 to 1 cm in diameter, spread over the entire body, sometimes including palms or soles, but never oral mucosa."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19139
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "HP:0000953",
          "ICD9:709.09",
          "MEDGEN:57992",
          "Orphanet:79375",
          "SCTID:49765009",
          "UMLS:C0162834"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 24,
      "reference_id": "MONDO:0019289"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin"
    }
  ]
}