{
  "id": 11537,
  "label": "premature ovarian failure 2B",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010373",
  "properties": {
    "xrefs": [
      "DOID:0080859",
      "GARD:0024721",
      "MEDGEN:337159",
      "MESH:C564476",
      "OMIM:300604",
      "UMLS:C1845105"
    ],
    "synonyms": [
      "POF1B primary ovarian failure",
      "premature ovarian failure 2B",
      "premature ovarian failure 2B, X-linked recessive",
      "premature ovarian failure type 2B",
      "primary ovarian failure caused by mutation in POF1B",
      "POF2B"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any primary ovarian failure in which the cause of the disease is a mutation in the POF1B gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19578,
      "label": "inherited primary ovarian failure",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7067,
        16330,
        20362
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019294",
          "MEDGEN:443920",
          "OMIMPS:311360",
          "Orphanet:95710",
          "UMLS:C2930861"
        ],
        "synonyms": [
          "hereditary primary ovarian failure",
          "inherited POI",
          "inherited premature ovarian failure",
          "inherited primary ovarian insufficiency",
          "non-acquired premature ovarian failure"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An instance of primary ovarian failure that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 164,
      "reference_id": "MONDO:0019852"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19578,
      "label": "inherited primary ovarian failure"
    }
  ]
}