{
  "id": 9035,
  "label": "hyperglycinuria",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007677",
  "properties": {
    "xrefs": [
      "HP:0003108",
      "MEDGEN:107456",
      "MESH:C563009",
      "OMIM:138500",
      "UMLS:C0543541"
    ],
    "synonyms": [
      "hyperglycinuria",
      "hyperglycinuria (disease)",
      "Iminoglycinuria type 2",
      "glycinuria with or without oxalate nephrolithiasis",
      "glycinuria with or without oxalate urolithiasis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4253,
      "label": "urinary system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:18",
          "EFO:0009690",
          "ICD9:V47.4",
          "MEDGEN:21791",
          "MESH:D014570",
          "NCIT:C3430",
          "SCTID:128606002",
          "UMLS:C0042075"
        ],
        "synonyms": [
          "disease of renal system",
          "disease or disorder of renal system",
          "disease, urinary tract",
          "disease, urologic",
          "disease, urological",
          "diseases, urinary tract",
          "diseases, urologic",
          "diseases, urological",
          "disorder of renal system",
          "disorder of the urinary system",
          "disorder of urinary system",
          "renal system disease",
          "renal system disease or disorder",
          "urinary disease",
          "urinary system disorder",
          "urinary tract disease",
          "urinary tract diseases",
          "urinary tract disorder",
          "urologic disease",
          "urologic disorder",
          "urological disease",
          "urological diseases",
          "urological disorder",
          "urological disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          }
        ],
        "definition": "A disease involving the renal system."
      },
      "child_count": 20,
      "reference_id": "MONDO:0002118"
    },
    {
      "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": 4253,
      "label": "urinary system disorder"
    },
    {
      "id": 5714,
      "label": "hereditary disease"
    }
  ]
}