{
  "id": 24970,
  "label": "46,XX true hermaphroditism, SRY-positive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0800381",
  "properties": {
    "xrefs": [
      "GARD:0026536"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17857,
      "label": "46,XX disorder of sex development",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4277
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018783",
          "MEDGEN:424728",
          "MESH:D058489",
          "NCIT:C127169",
          "Orphanet:2982",
          "SCTID:8800006",
          "UMLS:C2936403"
        ],
        "synonyms": [
          "46,XX DSD",
          "46,XX differences of Sex development",
          "46,XX disorders of Sex development",
          "female pseudohermaphroditism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Conditions affecting individuals with 46,XX karyotype characterized by atypical development of one or more of the following: the gonads, the internal reproductive structures, the external reproductive/genital structures."
      },
      "child_count": 6,
      "reference_id": "MONDO:0017576"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17857,
      "label": "46,XX disorder of sex development"
    }
  ]
}