{
  "id": 20128,
  "label": "nephrolithiasis susceptibility caused by SLC26A1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020722",
  "properties": {
    "xrefs": [
      "DOID:0080652",
      "MEDGEN:1830325",
      "OMIM:167030",
      "UMLS:C5779632"
    ],
    "synonyms": [
      "CAON",
      "nephrolithiasis, calcium oxalate",
      "urolithiasis, calcium oxalate"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20011,
      "label": "inherited disease susceptibility",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23063
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Z15",
          "MEDGEN:1876499",
          "MESH:D020022",
          "UMLS:C1455997"
        ],
        "synonyms": [
          "hereditary disease susceptibility",
          "hereditary predisposition to disease",
          "genetic predisposition",
          "genetic predispositions",
          "genetic susceptibilities",
          "genetic susceptibility",
          "predisposition, genetic",
          "predispositions, genetic",
          "susceptibilities, genetic",
          "susceptibility, genetic"
        ],
        "definition": "A latent susceptibility to disease at the genetic level, which may be activated under certain conditions."
      },
      "child_count": 284,
      "reference_id": "MONDO:0020573"
    },
    {
      "id": 25654,
      "label": "nephrolithiasis, calcium oxalate",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9482,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:318935",
          "OMIMPS:167030",
          "UMLS:C1833683"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0957318"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20011,
      "label": "inherited disease susceptibility"
    },
    {
      "id": 25654,
      "label": "nephrolithiasis, calcium oxalate"
    }
  ]
}