{
  "id": 10652,
  "label": "hypogonadism, male",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009421",
  "properties": {
    "xrefs": [
      "ICD9:257.2",
      "MEDGEN:57480",
      "OMIM:241100",
      "SCTID:48723006",
      "UMLS:C0151721"
    ],
    "synonyms": [
      "hypogonadism, male",
      "hypogonadism and testicular atrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4278,
      "label": "hypogonadism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4375
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1924",
          "ICD9:253.4",
          "MEDGEN:5711",
          "MESH:D007006",
          "NCIT:C9227",
          "SCTID:48130008",
          "UMLS:C0020619"
        ],
        "synonyms": [
          "gonadotropin deficiency",
          "hypogonadotropism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disorder characterized by decreased function of the gonads. Clinical manifestations in both males and females include poor libido, infertility, and osteoporosis. Additional signs in males include erectile dysfunction, muscle atrophy, gynecomastia and increased abdominal fat. In females, additional signs include shrinking of the breasts and loss of, or failure to develop menstruation."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002146"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 4278,
      "label": "hypogonadism"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}