{
  "id": 11794,
  "label": "major affective disorder 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010648",
  "properties": {
    "xrefs": [
      "DOID:0080221",
      "MEDGEN:326975",
      "MESH:C564108",
      "OMIM:309200",
      "UMLS:C1839839"
    ],
    "synonyms": [
      "MAFD2",
      "major affective disorder 2",
      "major affective disorder 2, X-linked dominant",
      "MAJOR affective disorder 2",
      "bipolar affective disorder",
      "manic-depressive illness",
      "manic-depressive psychosis, X-linked"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3086,
      "label": "bipolar II disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6726
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060166",
          "ICD10CM:F31.81",
          "ICD9:296.89",
          "MEDGEN:536634",
          "SCTID:83225003",
          "UMLS:C0236788"
        ],
        "synonyms": [
          "bipolar II disorder",
          "bipolar 2 disorder",
          "bipolar ll disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A bipolar disorder that is characterized by at least one hypomanic episode and at least one major depressive episode; with this disorder, depressive episodes are more frequent and more intense than manic episodes."
      },
      "child_count": 1,
      "reference_id": "MONDO:0000693"
    },
    {
      "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": 3086,
      "label": "bipolar II disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}