{
  "id": 15245,
  "label": "testicular anomalies with or without congenital heart disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014239",
  "properties": {
    "xrefs": [
      "GARD:0018360",
      "MEDGEN:816188",
      "OMIM:615542",
      "UMLS:C3809858"
    ],
    "synonyms": [
      "testicular anomalies with or without congenital heart disease",
      "TACHD"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 17141,
      "label": "46,XY partial gonadal dysgenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19710
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017211",
          "MEDGEN:1388250",
          "Orphanet:251510",
          "SCTID:725045004",
          "UMLS:C4510744"
        ],
        "synonyms": [
          "46,XY PGD",
          "46,XY partial testicular dysgenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "46,XY partial gonadal dysgenesis (46,XY PGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that results in genital ambiguity of variable degree ranging from almost female phenotype to almost male phenotype in a patient carrying a male 46,XY karyotype."
      },
      "child_count": 7,
      "reference_id": "MONDO:0016674"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 17141,
      "label": "46,XY partial gonadal dysgenesis"
    }
  ]
}