{
  "id": 14536,
  "label": "schizophrenia 16",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013506",
  "properties": {
    "xrefs": [
      "DOID:0070092",
      "MEDGEN:462758",
      "OMIM:613959",
      "UMLS:C3151408"
    ],
    "synonyms": [
      "SCZD16",
      "schizophrenia 16",
      "schizophrenia type 16",
      "chromosome 7Q36.3 Duplication syndrome, 362-Kb",
      "schizophrenia susceptibility locus, chromosome 7Q36.3-related"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A schizophrenia that has material basis in a mutation on chromosome 7q36.3."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3606,
      "label": "myopia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6646,
        24305
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11830",
          "HP:0000545",
          "ICD10CM:H52.1",
          "ICD9:367.1",
          "MEDGEN:44558",
          "MESH:D009216",
          "OMIMPS:160700",
          "SCTID:57190000",
          "UMLS:C0027092",
          "icd11.foundation:1666440799"
        ],
        "synonyms": [
          "myopia",
          "myopia (disease)",
          "near-sightedness"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The condition in which the individual does not see far distances clearly."
      },
      "child_count": 90,
      "reference_id": "MONDO:0001384"
    },
    {
      "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": 3606,
      "label": "myopia"
    },
    {
      "id": 6817,
      "label": "schizophrenia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}