{
  "id": 14534,
  "label": "spermatogenic failure 8",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013504",
  "properties": {
    "xrefs": [
      "DOID:0070169",
      "GARD:0015734",
      "MEDGEN:462756",
      "OMIM:613957",
      "UMLS:C3151406"
    ],
    "synonyms": [
      "NR5A1 azoospermia",
      "azoospermia caused by mutation in NR5A1",
      "spermatogenic failure 8",
      "spermatogenic failure type 8",
      "SPGF8"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      }
    ],
    "definition": "Any azoospermia in which the cause of the disease is a mutation in the NR5A1 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6724,
      "label": "spermatogenic failure",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7053
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111910",
          "EFO:0000279",
          "MEDGEN:766708",
          "OMIMPS:258150",
          "UMLS:C3553794"
        ],
        "synonyms": [
          "spermatogenic failure"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A male infertility characterized by dirsuption of the process of sperm development from diploid cells into mature haploid spermatozoa."
      },
      "child_count": 226,
      "reference_id": "MONDO:0004983"
    },
    {
      "id": 29369,
      "label": "NR5A1-related sex development disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6772
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "NR5A1-related sex development disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A reproductive system disorder caused by a variation in the NR5A1 gene, and characterized by varying phenotypes, including partial or complete gonadal dysgenesis, ambiguous genitalia, and spermatogenic failure in the male, and premature ovarian failure and ovarian dysgenesis in the female."
      },
      "child_count": 8,
      "reference_id": "MONDO:1060211"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6724,
      "label": "spermatogenic failure"
    },
    {
      "id": 29369,
      "label": "NR5A1-related sex development disorder"
    }
  ]
}