{
  "id": 8530,
  "label": "isolated anhidrosis with normal sweat glands",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007118",
  "properties": {
    "xrefs": [
      "DOID:0060603",
      "GARD:0017843",
      "MEDGEN:1800259",
      "OMIM:106190",
      "Orphanet:468666",
      "UMLS:C5568836"
    ],
    "synonyms": [
      "Dann-Epstein-Sohar syndrome",
      "ITPR2 anhidrosis",
      "anhidrosis caused by mutation in ITPR2",
      "ANHD",
      "anhidrosis, isolated, with normal sweat glands",
      "isolated generalised anhidrosis with normal sweat glands",
      "isolated generalized anhidrosis with normal sweat glands"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any anhidrosis in which the cause of the disease is a mutation in the ITPR2 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8014,
      "label": "anhidrosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8090
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11156",
          "EFO:1000670",
          "ICD10CM:L74.4",
          "ICD9:705.0",
          "MEDGEN:1550",
          "SCTID:39659002",
          "UMLS:C0003028"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Lack of sweating or the ability to sweat when provoked by the appropriate stimulus."
      },
      "child_count": 2,
      "reference_id": "MONDO:0006527"
    },
    {
      "id": 19144,
      "label": "subcutaneous tissue disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4198
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:712397",
          "Orphanet:79382",
          "UMLS:C1290008"
        ],
        "synonyms": [
          "disease of superficial fascia",
          "disease or disorder of superficial fascia",
          "disorder of superficial fascia",
          "superficial fascia disease",
          "superficial fascia disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease involving the superficial fascia."
      },
      "child_count": 19,
      "reference_id": "MONDO:0019296"
    },
    {
      "id": 20387,
      "label": "dermis disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1843083",
          "Orphanet:79381",
          "UMLS:C5681483"
        ],
        "synonyms": [
          "dermis disease",
          "dermis disease or disorder",
          "disease of dermis",
          "disease or disorder of dermis",
          "disorder of dermis",
          "other dermis disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease that involves the dermis."
      },
      "child_count": 28,
      "reference_id": "MONDO:0021154"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 8014,
      "label": "anhidrosis"
    },
    {
      "id": 19144,
      "label": "subcutaneous tissue disorder"
    },
    {
      "id": 20387,
      "label": "dermis disorder"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}