{
  "id": 23112,
  "label": "Zazam Sheriff Phillips syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043071",
  "properties": {
    "xrefs": [
      "GARD:0027966",
      "MEDGEN:419768",
      "MESH:C536723",
      "UMLS:C2931300"
    ],
    "synonyms": [
      "aniridia, ectopia lentis, abnormal upper incisors and intellectual disability",
      "aniridia, ectopia lentis, abnormal upper incisors and mental retardation",
      "aniridia, lens luxation, intellectual disability",
      "aniridia, lens luxation, mental retardation"
    ],
    "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": 19047,
      "label": "aniridia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4401,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12271",
          "GARD:0027869",
          "ICD10CM:Q13.1",
          "ICD9:743.45",
          "MEDGEN:1941",
          "MESH:D015783",
          "MedDRA:10002532",
          "NANDO:1201001",
          "NCIT:C84563",
          "Orphanet:77",
          "SCTID:69278003",
          "UMLS:C0003076",
          "icd11.foundation:970699895"
        ],
        "synonyms": [
          "aplasia of iris"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Aniridia is a congenital ocular malformation characterized by the complete or partial absence of the iris. It can be isolated or part of a syndrome (isolated and syndromic aniridia)."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019172"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 19047,
      "label": "aniridia"
    }
  ]
}