{
  "id": 14718,
  "label": "chromosome 2p16.3 deletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013696",
  "properties": {
    "xrefs": [
      "GARD:0024940",
      "MEDGEN:814824",
      "OMIM:614332",
      "UMLS:C3808494"
    ],
    "synonyms": [
      "chromosome 2P16.3 deletion syndrome",
      "schizophrenia, susceptibility to, 17"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6817,
      "label": "schizophrenia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7141
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5419",
          "HP:0100753",
          "ICD10CM:F20",
          "ICD10WHO:F20",
          "ICD9:295",
          "ICD9:295.8",
          "ICD9:295.80",
          "ICD9:295.85",
          "ICD9:295.9",
          "ICD9:295.90",
          "MEDGEN:48574",
          "NCIT:C3362",
          "OMIM:181500",
          "Orphanet:3140",
          "SCTID:58214004",
          "UMLS:C0036341",
          "birnlex:2104",
          "icd11.foundation:1683919430"
        ],
        "synonyms": [
          "schizophrenia 12",
          "schizophrenia",
          "schizophrenia (disease)",
          "SCZD",
          "schizoaffective disorder",
          "schizophrenia with or without an affective disorder",
          "schizophrenia, susceptibility to"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A major psychotic disorder characterized by abnormalities in the perception or expression of reality. It affects the cognitive and psychomotor functions. Common clinical signs and symptoms include delusions, hallucinations, disorganized thinking, and retreat from reality."
      },
      "child_count": 18,
      "reference_id": "MONDO:0005090"
    },
    {
      "id": 17309,
      "label": "partial deletion of the short arm of chromosome 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1826019",
          "Orphanet:261866",
          "UMLS:C5679664",
          "icd11.foundation:1610083208"
        ],
        "synonyms": [
          "partial deletion of chromosome 2p",
          "partial deletion of the short arm of chromosome type 2",
          "partial monosomy of chromosome 2p",
          "partial monosomy of the short arm of chromosome 2"
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0016884"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6817,
      "label": "schizophrenia"
    },
    {
      "id": 17309,
      "label": "partial deletion of the short arm of chromosome 2"
    }
  ]
}