{
  "id": 8870,
  "label": "dyschromatosis symmetrica hereditaria",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007483",
  "properties": {
    "xrefs": [
      "DOID:0060257",
      "GARD:0000334",
      "MEDGEN:96071",
      "MESH:C535729",
      "NCIT:C118435",
      "OMIM:127400",
      "Orphanet:41",
      "SCTID:239085000",
      "UMLS:C0406775"
    ],
    "synonyms": [
      "DSH1",
      "RAD",
      "acropigmentation of Dohi",
      "dyschromatosis symmetrica hereditaria",
      "reticulate acropigmentation of Dohi",
      "DSH",
      "dyschromatosis symmetrica hereditaria 1",
      "familial reticulate acropigmentation of Dohi",
      "symmetric dyschromatosis of the extremities"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      }
    ],
    "definition": "Acropigmentation of Dohi is a genodermatosis characterized by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs."
  },
  "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"
    },
    {
      "id": 24656,
      "label": "ADAR-related type 1 interferonopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21247,
        24659
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026404"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          }
        ],
        "definition": "Any type 1 interferonopathies in which the cause of the disease is a variation in the ADAR gene. Individuals with variants in ADAR can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and dyschromatosis symmetrica hereditaria."
      },
      "child_count": 4,
      "reference_id": "MONDO:0700261"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2731,
      "label": "reticulate pigment disorder"
    },
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin"
    },
    {
      "id": 24656,
      "label": "ADAR-related type 1 interferonopathy"
    }
  ]
}