{
  "id": 9144,
  "label": "chromosome 18p deletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007800",
  "properties": {
    "xrefs": [
      "DOID:0060406",
      "GARD:0020818",
      "ICD9:758.39",
      "MEDGEN:96604",
      "MESH:C538309",
      "NCIT:C84521",
      "OMIM:146390",
      "Orphanet:1598",
      "Orphanet:261974",
      "SCTID:270890001",
      "UMLS:C0432442",
      "icd11.foundation:121037615"
    ],
    "synonyms": [
      "18p syndrome",
      "18p-",
      "chromosome 18p deletion",
      "chromosome 18p deletion syndrome",
      "deletion 18p syndrome",
      "monosomy type 18p",
      "partial deletion of chromosome 18p",
      "partial deletion of the short arm of chromosome 18",
      "partial deletion of the short arm of chromosome type 18",
      "partial monosomy of chromosome 18p",
      "partial monosomy of the short arm of chromosome 18"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18."
  },
  "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": 17305,
      "label": "partial deletion of chromosome 18",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3128,
        24520
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1826018",
          "Orphanet:261836",
          "UMLS:C5679660"
        ],
        "synonyms": [
          "partial deletion of chromosome type 18",
          "partial monosomy of chromosome 18"
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0016880"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 17305,
      "label": "partial deletion of chromosome 18"
    }
  ]
}