{
  "id": 10298,
  "label": "cryptorchidism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009047",
  "properties": {
    "xrefs": [
      "DOID:11383",
      "EFO:0004562",
      "HP:0000028",
      "ICD9:752.5",
      "ICD9:752.51",
      "MEDGEN:8192",
      "MESH:D003456",
      "NCIT:C12326",
      "OMIM:219050",
      "SCTID:204878001",
      "UMLS:C0010417",
      "icd11.foundation:1134950387"
    ],
    "synonyms": [
      "cryptorchidism",
      "cryptorchidism (disease)",
      "undescended testes",
      "undescended testicle",
      "undescended testis",
      "cryptorchidism, unilateral or bilateral"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      }
    ],
    "definition": "The failure of one or both testes of a male fetus to descend from the abdomen into the scrotum during the late part of pregnancy. If not surgically corrected in early childhood, males may be at increased risk for testicular cancer later in life."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 5121,
      "label": "male reproductive system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6772
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:48",
          "EFO:0009555",
          "ICD10CM:N40-N53",
          "ICD10WHO:N40-N51",
          "ICD9:600-608",
          "ICD9:608.9",
          "MEDGEN:66734",
          "MESH:D005832",
          "NCIT:C27019",
          "SCTID:363194005",
          "UMLS:C0236099"
        ],
        "synonyms": [
          "Male reproductive system disease",
          "Male reproductive system disorder",
          "disease of male reproductive system",
          "disease or disorder of male reproductive system",
          "disorder of Male reproductive system",
          "disorder of male reproductive system",
          "male reproductive disease",
          "male reproductive system disease",
          "male reproductive system disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A disease involving the male reproductive system."
      },
      "child_count": 26,
      "reference_id": "MONDO:0003150"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 20780,
      "label": "Arroyo Garcia Cimadevilla syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3301,
        10298
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:419817",
          "MESH:C537439",
          "UMLS:C2931494"
        ],
        "synonyms": [
          "bilateral anophthalmia, esophageal atresia, and right cryptorchidism"
        ],
        "categories": [
          {
            "ref": "MONDO:0004335",
            "name": "digestive system disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          }
        ],
        "definition": "A syndrome characterized by bilateral anophthalmia (absence of one or both eyes), esophageal atresia (the upper esophagus ends and does not connect with the lower esophagus and stomach), and cryptorchidism (a condition in which one or both of the testes fail to descend from the abdomen into the scrotum). This is an n-of-1 use case where only one patient or family has been described with this disorder."
      },
      "child_count": 0,
      "reference_id": "MONDO:0021923"
    }
  ],
  "roots": [
    {
      "id": 5121,
      "label": "male reproductive system disorder"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}