{
  "id": 20891,
  "label": "bhaskar jagannathan syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022567",
  "properties": {
    "xrefs": [
      "MEDGEN:419280",
      "MESH:C535437",
      "UMLS:C2930901"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "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": 6853,
      "label": "cataract",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3420,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:83",
          "HP:0000518",
          "ICD9:366",
          "ICD9:366.44",
          "ICD9:366.8",
          "ICD9:366.9",
          "MEDGEN:39462",
          "MESH:D002386",
          "NCIT:C26713",
          "OMIMPS:116200",
          "SCTID:193570009",
          "UMLS:C0086543",
          "icd11.foundation:109841337"
        ],
        "synonyms": [
          "cataract",
          "cataract (disease)",
          "opacity of the lens"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Partial or complete opacity of the crystalline lens of one or both eyes that decreases visual acuity and eventually results in blindness. Some cataracts appear in infancy or in childhood, but most develop in older individuals. (Sternberg Diagnostic Surgical Pathology, 3rd ed.)"
      },
      "child_count": 58,
      "reference_id": "MONDO:0005129"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 6853,
      "label": "cataract"
    }
  ]
}