{
  "id": 23988,
  "label": "46,XX sex reversal 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100250",
  "properties": {
    "xrefs": [
      "DOID:0111761",
      "GARD:0026098",
      "MEDGEN:411324",
      "NCIT:C179867",
      "OMIM:400045",
      "UMLS:C2748895"
    ],
    "synonyms": [
      "ovotesticular DSD",
      "ovotesticular disorder of sex development",
      "46,XX SEX reversal 1",
      "46,XX Sex reversal type 1",
      "46,XX Sex reversal, SRY-positive",
      "46,XX gonadal dysgenesis, complete, SRY-positive",
      "46XX sex reversal 1, X-linked dominant",
      "SRXX1",
      "46,XX true hermaphroditism, SRY-positive"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 23987,
      "label": "46,XX testicular disorder of sex development",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17857
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111760",
          "GARD:0000399",
          "MEDGEN:424734",
          "MESH:D058531",
          "NCIT:C127170",
          "Orphanet:393",
          "UMLS:C2936419",
          "icd11.foundation:1357942532"
        ],
        "synonyms": [
          "46,XX testicular DSD",
          "46,XX testicular differences of sex development",
          "46,XX testicular disorder of sex development",
          "46,XX testicular disorders of Sex development",
          "De la Chapelle syndrome",
          "XX, male syndrome",
          "46, XX gonadal sex reversal",
          "XX Male, Sry-positive",
          "XX male syndrome",
          "XX sex reversal"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "46,XX testicular disorder of sex development (46,XX testicular DSD) is characterized by male external genitalia, ranging from normal to ambiguous with associated testosterone deficiency."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100249"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 23987,
      "label": "46,XX testicular disorder of sex development"
    }
  ]
}