{
  "id": 14528,
  "label": "schizophrenia 15",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013498",
  "properties": {
    "xrefs": [
      "DOID:0070091",
      "MEDGEN:462730",
      "OMIM:613950",
      "UMLS:C3151380"
    ],
    "synonyms": [
      "SCZD15",
      "schizophrenia 15",
      "schizophrenia type 15",
      "schizophrenia 15 with or without an affective disorder",
      "schizophrenia susceptibility locus, chromosome 22Q13-related"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A schizophrenia that has material basis in a mutation of SHANK3 on chromosome 22q13.33."
  },
  "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": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6817,
      "label": "schizophrenia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}