{
  "id": 23235,
  "label": "Leriche syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043683",
  "properties": {
    "xrefs": [
      "MEDGEN:44114",
      "MESH:D007925",
      "NCIT:C34773",
      "SCTID:307816004",
      "UMLS:C0023370"
    ],
    "synonyms": [
      "Leriche syndrome",
      "leriche's syndrome",
      "Leriche's syndrome",
      "Leriches syndrome",
      "syndrome, Leriche",
      "syndrome, Leriche's"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "An atherosclerotic disorder of the peripheral vascular system affecting mostly males in their later decades. It is caused by thrombotic occlusion of the abdominal aorta just above the level of the bifurcation. Clinical signs include impotence, intermittent claudication, diminished femoral pulses and cold, pallid lower extremities. Prognosis is favorable with surgical or endovascular intervention."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 7210,
      "label": "aortic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:520",
          "EFO:0005775",
          "ICD9:447.9",
          "MEDGEN:1618",
          "MESH:D001018",
          "NCIT:C101253",
          "SCTID:47040006",
          "UMLS:C0003493"
        ],
        "synonyms": [
          "aorta disease",
          "aorta disease or disorder",
          "disease of aorta",
          "disease or disorder of aorta",
          "disorder of aorta"
        ],
        "categories": [
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Pathology involving the thoracic, thoracoabdominal, or abdominal aorta (including aneurysms). (ACC)"
      },
      "child_count": 17,
      "reference_id": "MONDO:0005561"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 7210,
      "label": "aortic disorder"
    }
  ]
}