{
  "id": 6724,
  "label": "spermatogenic failure",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0004983",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 113,
  "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": 7053,
      "label": "male infertility",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5121,
        6779
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12336",
          "EFO:0004248",
          "ICD10CM:N46",
          "ICD10WHO:N46",
          "ICD9:606",
          "ICD9:606.9",
          "MEDGEN:5796",
          "MESH:D007248",
          "SCTID:2904007",
          "UMLS:C0021364",
          "icd11.foundation:753457327"
        ],
        "synonyms": [
          "infertility disorder of male reproductive system",
          "male reproductive system infertility",
          "male reproductive system infertility disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "The inability of the male to effect fertilization of an ovum after a specified period of unprotected intercourse. Male sterility is permanent infertility."
      },
      "child_count": 16,
      "reference_id": "MONDO:0005372"
    }
  ],
  "children": [
    {
      "id": 8479,
      "label": "spermatogenic failure 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        16506
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070167",
          "GARD:0015032",
          "MEDGEN:900925",
          "OMIM:102530",
          "SCTID:236818008",
          "UMLS:C4225503"
        ],
        "synonyms": [
          "SPATA16 azoospermia",
          "azoospermia caused by mutation in SPATA16",
          "spermatogenic failure 6",
          "spermatogenic failure type 6",
          "SPGF6",
          "acrosome malformation of spermatozoa",
          "globozoospermia",
          "round-headed spermatozoa",
          "spermatozoa, round-headed"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SPATA16 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007060"
    },
    {
      "id": 8568,
      "label": "spermatogenic failure 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070164",
          "GARD:0015041",
          "MEDGEN:400056",
          "OMIM:108420",
          "UMLS:C1862459"
        ],
        "synonyms": [
          "SPGF2",
          "spermatogenic failure 2",
          "Aspermiogenesis Factor"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007161"
    },
    {
      "id": 10688,
      "label": "spermatogenic failure 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        18463
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070183",
          "GARD:0012385",
          "MEDGEN:98020",
          "MESH:C562903",
          "OMIM:243060",
          "Orphanet:137893",
          "SCTID:236806004",
          "UMLS:C0403812"
        ],
        "synonyms": [
          "SPGF5",
          "macrocephalic sperm head syndrome",
          "macrozoospermia with multiflagellar polyploid spermatozoa",
          "male infertility due to large-headed multiflagellar polyploid spermatozoa",
          "male infertility due to macrozoospermia",
          "male infertility with large-headed, multiflagellar, polyploid spermatozoa",
          "spermatogenic failure 5",
          "spermatogenic failure type 5",
          "macrozoospermia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A male infertility due to sperm disorder characterized by the presence, in sperm, of a very high percentage of spermatozoa with enlarged head, irregular head shape, multiple flagella, and abnormal midpiece and acrosome. It is generally associated with severe oligoasthenozoospermia and a high rate of sperm chromosomal abnormalities (polyploidy, aneuploidy)."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009461"
    },
    {
      "id": 10986,
      "label": "spermatogenic failure 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070188",
          "GARD:0015214",
          "MEDGEN:140793",
          "MESH:C562902",
          "OMIM:258150",
          "SCTID:236803007",
          "UMLS:C0403810"
        ],
        "synonyms": [
          "SPGF1",
          "spermatogenic failure 1",
          "Oligochiasmatic infertility",
          "Oligosynaptic infertility"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009776"
    },
    {
      "id": 11243,
      "label": "spermatogenic failure 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070176",
          "GARD:0015235",
          "MEDGEN:68568",
          "MESH:C536875",
          "OMIM:270960",
          "UMLS:C0232981"
        ],
        "synonyms": [
          "SYCP3 azoospermia",
          "azoospermia caused by mutation in SYCP3",
          "spermatogenic failure 4",
          "spermatogenic failure type 4",
          "SPGF4",
          "arrest of spermatogenesis",
          "azoospermia due to Perturbations of meiosis",
          "azoospermia with maturation arrest",
          "pregnancy loss, recurrent, 4",
          "pregnancy loss, recurrent, susceptibility to, 4",
          "spermatogenesis arrest"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SYCP3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010052"
    },
    {
      "id": 11793,
      "label": "spermatogenic failure, X-linked, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070185",
          "GARD:0015302",
          "MEDGEN:374322",
          "OMIM:309120",
          "UMLS:C1839841"
        ],
        "synonyms": [
          "TEX11 azoospermia",
          "azoospermia caused by mutation in TEX11",
          "spermatogenic failure, X-linked, 2",
          "spermatogenic failure, X-linked, 2, X-linked recessive",
          "spermatogenic failure, X-linked, type 2",
          "Male infertility from defect in meiosis",
          "SPGFX2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the TEX11 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010647"
    },
    {
      "id": 11902,
      "label": "spermatogenic failure, Y-linked, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        16401
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010763"
    },
    {
      "id": 11905,
      "label": "spermatogenic failure, Y-linked, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        16401
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070187",
          "GARD:0018504",
          "MEDGEN:326394",
          "MESH:C564030",
          "OMIM:415000",
          "UMLS:C1839071"
        ],
        "synonyms": [
          "spermatogenic failure, Y-linked, 2",
          "spermatogenic failure, Y-linked, 2, Y-linked",
          "spermatogenic failure, Y-linked, type 2",
          "Azf regions",
          "SPGFY2",
          "azoospermia Factor regions",
          "azoospermia, nonobstructive, Y-linked",
          "oligospermia, nonobstructive, Y-linked",
          "oligozoospermia, nonobstructive, Y-linked",
          "spermatogenic arrest, Y-linked",
          "spermatogenic failure, nonobstructive, Y-linked"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010767"
    },
    {
      "id": 12807,
      "label": "spermatogenic failure 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070168",
          "GARD:0018399",
          "MEDGEN:1648302",
          "MESH:C564665",
          "OMIM:606766",
          "UMLS:C4721889"
        ],
        "synonyms": [
          "SLC26A8 azoospermia",
          "azoospermia caused by mutation in SLC26A8",
          "spermatogenic failure 3",
          "spermatogenic failure type 3",
          "SPGF3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SLC26A8 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011720"
    },
    {
      "id": 14108,
      "label": "spermatogenic failure 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070173",
          "GARD:0018400",
          "MEDGEN:414478",
          "MESH:C567832",
          "OMIM:612997",
          "UMLS:C2751811"
        ],
        "synonyms": [
          "spermatogenic failure 7",
          "spermatogenic failure type 7",
          "Male infertility, nonsyndromic, autosomal recessive",
          "SPGF7"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013070"
    },
    {
      "id": 14534,
      "label": "spermatogenic failure 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        29369
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013504"
    },
    {
      "id": 14535,
      "label": "spermatogenic failure 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        16506
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070175",
          "DOID:0111156",
          "GARD:0015735",
          "MEDGEN:462757",
          "OMIM:613958",
          "UMLS:C3151407"
        ],
        "synonyms": [
          "DPY19L2 azoospermia",
          "azoospermia caused by mutation in DPY19L2",
          "spermatogenic failure 9",
          "spermatogenic failure type 9",
          "SPGF9",
          "globozoospermia, complete",
          "globozoospermia, total"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the DPY19L2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013505"
    },
    {
      "id": 14913,
      "label": "spermatogenic failure 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070178",
          "GARD:0018401",
          "MEDGEN:766707",
          "OMIM:614822",
          "UMLS:C3553793"
        ],
        "synonyms": [
          "SEPT12 azoospermia",
          "azoospermia caused by mutation in SEPT12",
          "spermatogenic failure 10",
          "spermatogenic failure type 10",
          "SPGF10",
          "spermatogenic failure with defective sperm annulus"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SEPT12 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013901"
    },
    {
      "id": 15047,
      "label": "spermatogenic failure 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070180",
          "GARD:0015904",
          "MEDGEN:767367",
          "OMIM:615081",
          "UMLS:C3554453"
        ],
        "synonyms": [
          "KLHL10 azoospermia",
          "azoospermia caused by mutation in KLHL10",
          "spermatogenic failure 11",
          "spermatogenic failure type 11",
          "SPGF11"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the KLHL10 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014037"
    },
    {
      "id": 15179,
      "label": "spermatogenic failure 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        18463
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070171",
          "GARD:0015960",
          "MEDGEN:815757",
          "OMIM:615413",
          "UMLS:C3809427"
        ],
        "synonyms": [
          "NANOS1 azoospermia",
          "azoospermia caused by mutation in NANOS1",
          "spermatogenic failure 12",
          "spermatogenic failure type 12",
          "SPGF12"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the NANOS1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014172"
    },
    {
      "id": 15367,
      "label": "spermatogenic failure 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070182",
          "GARD:0016019",
          "MEDGEN:862886",
          "OMIM:615841",
          "UMLS:C4014449"
        ],
        "synonyms": [
          "TAF4B azoospermia",
          "azoospermia caused by mutation in TAF4B",
          "spermatogenic failure 13",
          "spermatogenic failure type 13",
          "SPGF13"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the TAF4B gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014365"
    },
    {
      "id": 15368,
      "label": "spermatogenic failure 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070179",
          "GARD:0016020",
          "MEDGEN:862891",
          "OMIM:615842",
          "UMLS:C4014454"
        ],
        "synonyms": [
          "ZMYND15 azoospermia",
          "azoospermia caused by mutation in ZMYND15",
          "spermatogenic failure 14",
          "spermatogenic failure type 14",
          "SPGF14"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the ZMYND15 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014366"
    },
    {
      "id": 15831,
      "label": "spermatogenic failure 15",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724,
        29372
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070172",
          "GARD:0016173",
          "MEDGEN:934746",
          "OMIM:616950",
          "UMLS:C4310779"
        ],
        "synonyms": [
          "SPGF15",
          "SYCE1 azoospermia",
          "azoospermia caused by mutation in SYCE1",
          "spermatogenic failure 15",
          "spermatogenic failure 15; SPGF15",
          "spermatogenic failure type 15"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SYCE1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014847"
    },
    {
      "id": 15940,
      "label": "spermatogenic failure 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070184",
          "MEDGEN:934641",
          "OMIM:617187",
          "UMLS:C4310674"
        ],
        "synonyms": [
          "SPGF16",
          "SUN5 azoospermia",
          "azoospermia caused by mutation in SUN5",
          "spermatogenic failure 16",
          "spermatogenic failure 16; SPGF16",
          "spermatogenic failure type 16",
          "acephalic spermatozoa syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the SUN5 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014961"
    },
    {
      "id": 15948,
      "label": "spermatogenic failure 17",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070174",
          "MEDGEN:934633",
          "OMIM:617214",
          "UMLS:C4310666"
        ],
        "synonyms": [
          "PLCZ1 azoospermia",
          "SPGF17",
          "azoospermia caused by mutation in PLCZ1",
          "spermatogenic failure 17",
          "spermatogenic failure 17; SPGF17",
          "spermatogenic failure type 17",
          "Male infertility due to oocyte Activation failure"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "Any azoospermia in which the cause of the disease is a mutation in the PLCZ1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014970"
    },
    {
      "id": 20232,
      "label": "spermatogenic failure 30",
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        "categories": [
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            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
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            "name": "reproductive system disorder"
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            "name": "reproductive system disorder"
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      },
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      "label": "spermatogenic failure 76",
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            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
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      "reference_id": "MONDO:0031083"
    },
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      "label": "spermatogenic failure 35",
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            "name": "reproductive system disorder"
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      "reference_id": "MONDO:0032686"
    },
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      "label": "spermatogenic failure 36",
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            "name": "reproductive system disorder"
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      },
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      "reference_id": "MONDO:0032739"
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      "label": "spermatogenic failure 37",
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            "name": "reproductive system disorder"
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        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032744"
    },
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      "label": "spermatogenic failure 38",
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            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032748"
    },
    {
      "id": 22500,
      "label": "spermatogenic failure 39",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
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      ],
      "type_id": 0,
      "properties": {
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            "name": "reproductive system disorder"
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      },
      "child_count": 0,
      "reference_id": "MONDO:0032845"
    },
    {
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      "label": "spermatogenic failure 40",
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      "parents": [
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            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032859"
    },
    {
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      "label": "spermatogenic failure 41",
      "isLeaf": true,
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      "parents": [
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      ],
      "type_id": 0,
      "properties": {
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            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032863"
    },
    {
      "id": 22548,
      "label": "spermatogenic failure 42",
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      "isRoot": false,
      "parents": [
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      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "SPGF42"
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        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032896"
    },
    {
      "id": 22550,
      "label": "spermatogenic failure 43",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111917",
          "GARD:0018414",
          "MEDGEN:1684830",
          "OMIM:618751",
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        ],
        "synonyms": [
          "SPERMATOGENIC FAILURE 43",
          "SPGF43"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032898"
    },
    {
      "id": 22703,
      "label": "spermatogenic failure 44",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "MEDGEN:1750188",
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        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033622"
    },
    {
      "id": 22735,
      "label": "spermatogenic failure 45",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112163",
          "MEDGEN:1776221",
          "OMIM:619094",
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        ],
        "synonyms": [
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        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033671"
    },
    {
      "id": 22737,
      "label": "spermatogenic failure 46",
      "isLeaf": true,
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      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
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        ],
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          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0033673"
    },
    {
      "id": 23572,
      "label": "spermatogenic failure 18",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070165",
          "GARD:0018402",
          "MEDGEN:1617309",
          "OMIM:617576",
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        ],
        "synonyms": [
          "spermatogenic failure 18",
          "SPGF18"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054615"
    },
    {
      "id": 23592,
      "label": "spermatogenic failure 19",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070170",
          "GARD:0018403",
          "MEDGEN:1614356",
          "OMIM:617592",
          "UMLS:C4539818"
        ],
        "synonyms": [
          "spermatogenic failure 19",
          "SPGF19"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054723"
    },
    {
      "id": 23593,
      "label": "spermatogenic failure 20",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "GARD:0018404",
          "MEDGEN:1621256",
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        ],
        "synonyms": [
          "spermatogenic failure 20",
          "SPGF20"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054724"
    },
    {
      "id": 23594,
      "label": "spermatogenic failure 21",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070163",
          "MEDGEN:1617056",
          "OMIM:617644",
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        ],
        "synonyms": [
          "spermatogenic failure 21",
          "SPGF21"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054725"
    },
    {
      "id": 23595,
      "label": "spermatogenic failure 22",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
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          "GARD:0016245",
          "MEDGEN:1618089",
          "OMIM:617706",
          "UMLS:C4540179"
        ],
        "synonyms": [
          "spermatogenic failure 22",
          "SPGF22"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054726"
    },
    {
      "id": 23596,
      "label": "spermatogenic failure 23",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070181",
          "GARD:0016246",
          "MEDGEN:1626589",
          "OMIM:617707",
          "UMLS:C4540185"
        ],
        "synonyms": [
          "spermatogenic failure 23",
          "SPGF23"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054727"
    },
    {
      "id": 23597,
      "label": "spermatogenic failure 24",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111929",
          "MEDGEN:1646063",
          "OMIM:617959",
          "UMLS:C4693751"
        ],
        "synonyms": [
          "spermatogenic failure 24",
          "SPGF24"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054728"
    },
    {
      "id": 23598,
      "label": "spermatogenic failure 25",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111920",
          "GARD:0016274",
          "MEDGEN:1646677",
          "OMIM:617960",
          "UMLS:C4693765"
        ],
        "synonyms": [
          "spermatogenic failure 25",
          "SPGF25"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054729"
    },
    {
      "id": 23599,
      "label": "spermatogenic failure 26",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111924",
          "MEDGEN:1644751",
          "OMIM:617961",
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        ],
        "synonyms": [
          "spermatogenic failure 26",
          "SPGF26"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054730"
    },
    {
      "id": 23600,
      "label": "spermatogenic failure 27",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111928",
          "GARD:0018405",
          "MEDGEN:1634748",
          "OMIM:617965",
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        ],
        "synonyms": [
          "spermatogenic failure 27",
          "SPGF27"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054731"
    },
    {
      "id": 23601,
      "label": "spermatogenic failure 28",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111916",
          "GARD:0016290",
          "MEDGEN:1648494",
          "OMIM:618086",
          "UMLS:C4748117"
        ],
        "synonyms": [
          "spermatogenic failure 28",
          "SPGF28"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054732"
    },
    {
      "id": 23602,
      "label": "spermatogenic failure 29",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111930",
          "MEDGEN:1648499",
          "OMIM:618091",
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        ],
        "synonyms": [
          "spermatogenic failure 29",
          "SPGF29"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054733"
    },
    {
      "id": 23658,
      "label": "X-linked spermatogenic failure 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070189",
          "GARD:0008406",
          "ICD9:752.89",
          "MEDGEN:235163",
          "MESH:D054331",
          "NCIT:C168988",
          "OMIM:305700",
          "SCTID:73465006",
          "UMLS:C1384583"
        ],
        "synonyms": [
          "Del Castillo syndrome",
          "Germinal cell aplasia",
          "SPGFX1",
          "Sertoli cell-only syndrome",
          "spermatogenic failure, X-linked, type 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A cause of male infertility characterized by X-linked inheritance in which only Sertoli cells (cells that nurture the immature sperm) line the seminiferous tubules (tubes inside the testicles where sperm develop) and there are not any sperm cells present in the seminiferous tubules."
      },
      "child_count": 0,
      "reference_id": "MONDO:0056795"
    },
    {
      "id": 24684,
      "label": "spermatogenic failure 98",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1876475",
          "OMIM:621124",
          "UMLS:C6012703"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0700290"
    },
    {
      "id": 25470,
      "label": "spermatogenic failure 78",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        6724
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070577",
          "MEDGEN:1824049",
          "OMIM:620170",
          "UMLS:C5774276"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859338"
    },
    {
      "id": 25479,
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}