{
  "id": 15240,
  "label": "reticulate acropigmentation of Kitamura",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014234",
  "properties": {
    "xrefs": [
      "DOID:0060258",
      "GARD:0017079",
      "ICD9:709.09",
      "MEDGEN:98363",
      "OMIM:615537",
      "Orphanet:178307",
      "SCTID:239133004",
      "UMLS:C0406811"
    ],
    "synonyms": [
      "reticulate acropigmentation of Kitamura",
      "Kitamura reticulate acropigmentation",
      "RAK",
      "acropigmentatio reticularis",
      "reticulate pigmentation of Kitamura"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A pigmentation disease characterized by lesions that initially arise as letiginous, hyperpigmented macules in a reticular pattern on the dorsal aspect of the hands and feet. Over time, lesions may spread proximally and may darken; palmoplantar pitting and dermatoglyphic disruption may also be present."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2731,
      "label": "reticulate pigment disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19139,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022712",
          "OMIMPS:179850"
        ],
        "synonyms": [
          "reticulate pigment disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0000118"
    },
    {
      "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": 2731,
      "label": "reticulate pigment disorder"
    },
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin"
    }
  ]
}