{
  "id": 19501,
  "label": "cystinuria type A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019745",
  "properties": {
    "xrefs": [
      "GARD:0016827",
      "MEDGEN:347441",
      "MESH:C565652",
      "Orphanet:93612",
      "UMLS:C1857388",
      "icd11.foundation:1172657361"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10317,
      "label": "cystinuria",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        16626,
        19084
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9266",
          "GARD:0006237",
          "HP:0003131",
          "ICD10CM:E72.01",
          "MEDGEN:8226",
          "MESH:D003555",
          "MedDRA:10011778",
          "NANDO:2200489",
          "NCIT:C84664",
          "OMIM:220100",
          "Orphanet:214",
          "SCTID:85020001",
          "UMLS:C0010691",
          "icd11.foundation:1237620397"
        ],
        "synonyms": [
          "cystinuria",
          "cystinuria (disease)",
          "cystinuria-lysinuria syndrome",
          "CSNU",
          "cystinuria, type A/B",
          "cystinuria, type B",
          "cystinuria, type I",
          "cystinuria, type I, formerly",
          "cystinuria, type II",
          "cystinuria, type II, formerly",
          "cystinuria, type III",
          "cystinuria, type III, formerly",
          "cystinuria, type a",
          "cystinuria, type non-I",
          "cystinuria, type non-I, formerly",
          "cystinuria-lysinuria"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Cystinuria is a renal tubular amino acid transport disorder characterized by recurrent formation of kidneys cystine stones."
      },
      "child_count": 6,
      "reference_id": "MONDO:0009067"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10317,
      "label": "cystinuria"
    }
  ]
}