{
  "id": 3112,
  "label": "dyschromatosis universalis hereditaria",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000736",
  "properties": {
    "xrefs": [
      "DOID:0060304",
      "GARD:0001996",
      "MEDGEN:419691",
      "MESH:C535730",
      "NCIT:C173131",
      "OMIMPS:127500",
      "Orphanet:241",
      "SCTID:239082002",
      "UMLS:C2930995",
      "icd11.foundation:480710406"
    ],
    "synonyms": [
      "dyschromatosis universalis",
      "DUH"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "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"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 14033,
      "label": "dyschromatosis universalis hereditaria 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015581",
          "MEDGEN:382542",
          "MESH:C567194",
          "OMIM:612715",
          "UMLS:C2675183"
        ],
        "synonyms": [
          "dyschromatosis universalis hereditaria 2",
          "DUH2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012993"
    },
    {
      "id": 15176,
      "label": "dyschromatosis universalis hereditaria 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015959",
          "MEDGEN:815724",
          "OMIM:615402",
          "UMLS:C3809394"
        ],
        "synonyms": [
          "ABCB6 dyschromatosis universalis hereditaria",
          "dyschromatosis universalis hereditaria 3",
          "dyschromatosis universalis hereditaria caused by mutation in ABCB6",
          "dyschromatosis universalis hereditaria type 3",
          "DUH3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any dyschromatosis universalis hereditaria in which the cause of the disease is a mutation in the ABCB6 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014169"
    },
    {
      "id": 21470,
      "label": "dyschromatosis universalis hereditaria 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025411",
          "MEDGEN:390864",
          "MESH:C567273",
          "OMIM:127500",
          "UMLS:C2675711"
        ],
        "synonyms": [
          "DUH1",
          "dyschromatosis universalis hereditaria 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024524"
    }
  ],
  "roots": [
    {
      "id": 19140,
      "label": "hyperpigmentation of the skin"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}