{
  "id": 9664,
  "label": "Raynaud disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008364",
  "properties": {
    "xrefs": [
      "DOID:10300",
      "EFO:1001145",
      "ICD10CM:I73.0",
      "ICD9:443.0",
      "MEDGEN:20473",
      "MESH:D011928",
      "NCIT:C116359",
      "OMIM:179600",
      "SCTID:195295006",
      "UMLS:C0034734"
    ],
    "synonyms": [
      "Raynaud disease",
      "Raynaud syndrome",
      "Raynaud's disease",
      "Raynaud's syndrome",
      "Raynaud's syndrome (disorder) [ambiguous]",
      "secondary Raynaud disease",
      "secondary Raynaud phenomenon",
      "secondary Raynaud's disease",
      "secondary Raynaud's phenomenon",
      "cold fingers, hereditary"
    ],
    "categories": [
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "An episodic vasoconstriction resulting in discoloration of the skin and pain in the affected areas, often involving fingers or toes. Classically associated with triphasic color changes (white, blue, red) but may be biphasic. Often occurs in response to cold temperatures or emotional stress. May be primary or secondary to an underlying autoimmune disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6988,
      "label": "peripheral vascular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7065
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:341",
          "EFO:0003875",
          "ICD9:443.81",
          "MEDGEN:38790",
          "MESH:D016491",
          "NCIT:C35136",
          "UMLS:C0085096",
          "icd11.foundation:426429380"
        ],
        "synonyms": [
          "disease, peripheral vascular",
          "peripheral vascular disorder",
          "vascular disease, peripheral"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any disorder affecting blood flow through the veins or arteries outside of the heart."
      },
      "child_count": 11,
      "reference_id": "MONDO:0005294"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6988,
      "label": "peripheral vascular disease"
    }
  ]
}