{
  "id": 21419,
  "label": "ovarian dysgenesis 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024463",
  "properties": {
    "xrefs": [
      "DOID:0080493",
      "GARD:0018039",
      "MEDGEN:215397",
      "OMIM:233300",
      "UMLS:C0949595"
    ],
    "synonyms": [
      "ODG1",
      "ovarian dysgenesis 1",
      "XX gonadal dysgenesis",
      "XXGD",
      "gonadal dysgenesis, 20 type",
      "gonadal dysgenesis, XX type",
      "ovarian dysgenesis, hypergonadotropic, autosomal recessive",
      "ovarian dysgenesis, hypergonadotropic, with normal karyotype",
      "ovarian failure, hypergonadotropic"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10538,
      "label": "46 XX gonadal dysgenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4130,
        19578
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14450",
          "GARD:0005671",
          "MEDGEN:146899",
          "MESH:D023961",
          "NANDO:2200384",
          "NCIT:C120197",
          "OMIMPS:233300",
          "Orphanet:243",
          "SCTID:95198001",
          "UMLS:C0685837",
          "icd11.foundation:1742528605"
        ],
        "synonyms": [
          "46,XX complete gonadal dysgenesis",
          "46,XX gonadal dysgenesis",
          "46,XX ovarian dysgenesis",
          "46,XX pure gonadal dysgenesis",
          "FSH-RO",
          "XX female gonadal dysgenesis",
          "XX-GD",
          "follicular stimulating hormone-resistant ovaries",
          "hypergonadotropic ovarian dysgenesis",
          "XX gonadal dysgenesis",
          "ovarian dysgenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "46,XX gonadal dysgenesis (46,XX GD) is a primary ovarian defect leading to premature ovarian failure (POF) in otherwise normal 46,XX females as a result of failure of the gonads to develop or due to resistance to gonadotrophin stimulation."
      },
      "child_count": 22,
      "reference_id": "MONDO:0009299"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10538,
      "label": "46 XX gonadal dysgenesis"
    }
  ]
}