{
  "id": 9916,
  "label": "urticaria, familial localized heat",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008634",
  "properties": {
    "xrefs": [
      "MEDGEN:395922",
      "MESH:C566011",
      "OMIM:191950",
      "UMLS:C1860551"
    ],
    "synonyms": [
      "urticaria, familial localized heat"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7148,
      "label": "urticaria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1555",
          "EFO:0005531",
          "HP:0001025",
          "ICD10CM:L50",
          "ICD10WHO:L50",
          "ICD9:708",
          "ICD9:708.8",
          "ICD9:708.9",
          "MEDGEN:22587",
          "MESH:D014581",
          "NCIT:C3432",
          "SCTID:126485001",
          "UMLS:C0042109"
        ],
        "synonyms": [
          "hives",
          "urticaria",
          "urticaria (disease)",
          "Urticarias"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A vascular reaction of the skin characterized by erythema and wheal formation due to localized increase of vascular permeability. The causative mechanism may be allergy, infection, or stress."
      },
      "child_count": 14,
      "reference_id": "MONDO:0005492"
    },
    {
      "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": 7148,
      "label": "urticaria"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}