{
  "id": 11902,
  "label": "spermatogenic failure, Y-linked, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010763",
  "properties": {
    "xrefs": [
      "DOID:0070186",
      "GARD:0018503",
      "MEDGEN:1634798",
      "OMIM:400042",
      "UMLS:C4551960"
    ],
    "synonyms": [
      "spermatogenic failure, Y-linked, 1",
      "spermatogenic failure, Y-linked, 1, Y-linked",
      "spermatogenic failure, Y-linked, type 1",
      "SPGFY1",
      "Sertoli cell-only syndrome, Y-linked",
      "Sertoli cell-only syndrome, type 1",
      "Sertoli cell-only syndrome, type 2",
      "hypospermatogenesis",
      "incomplete Sertoli cell-only syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      }
    ]
  },
  "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": 16401,
      "label": "partial chromosome Y deletion",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3128,
        7053,
        24426
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016574",
          "HGNC:11311",
          "MEDGEN:267211",
          "MESH:C536297",
          "Orphanet:1646",
          "SCTID:717158001",
          "UMLS:C1507149"
        ],
        "synonyms": [
          "Male sterility due to chromosome Y deletion",
          "Y-chromosome microdeletions",
          "partial deletion of Y",
          "partial deletion of Y chromosome short arm",
          "partial deletion of chromosome Y",
          "partial deletion of the long arm of the Y chromosome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A genetic male infertility characterized by azoospermia or oligozoospermia due to chromosome Y microdeletion."
      },
      "child_count": 9,
      "reference_id": "MONDO:0015607"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6724,
      "label": "spermatogenic failure"
    },
    {
      "id": 16401,
      "label": "partial chromosome Y deletion"
    }
  ]
}