{
  "id": 18681,
  "label": "Holmes-Adie syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018690",
  "properties": {
    "xrefs": [
      "DOID:11549",
      "EFO:0004126",
      "GARD:0005749",
      "MEDGEN:138",
      "MESH:D000270",
      "NCIT:C34357",
      "NORD:735",
      "OMIM:103100",
      "Orphanet:454718",
      "SCTID:24225004",
      "UMLS:C0001519"
    ],
    "synonyms": [
      "Adie Syndrome",
      "Adie pupil",
      "Adie syndrome",
      "Adie's pupil",
      "Holmes-Adie syndrome",
      "tonic pupil",
      "tonic pupil-tendon areflexia syndrome",
      "poorly Reacting pupils",
      "tonic, sluggishly reacting pupil and hypoactive or absent tendon reflexes"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "A rare syndrome characterized by an abnormally dilated pupil, hypoflexia, and diaphoresis. The syndrome is usually caused by a viral or bacterial infection. The abnormally dilated pupil is caused by damage to postganglionic parasympathetic fibers innervating the eye."
  },
  "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}