{
  "id": 20042,
  "label": "Liddle syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020607",
  "properties": {
    "xrefs": [
      "GARD:0025186",
      "OMIM:177200"
    ],
    "synonyms": [
      "Liddle syndrome 1",
      "Liddle syndrome caused by mutation in SCNN1B",
      "SCNN1B Liddle syndrome",
      "LIDLS1",
      "Liddle syndrome",
      "Pseudoaldosteronism"
    ],
    "categories": [
      {
        "ref": "MONDO:0002118",
        "name": "urinary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Any Liddle syndrome in which the cause of the disease is a mutation in the SCNN1B gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9629,
      "label": "Liddle syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        8001,
        23932
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050477",
          "GARD:0007381",
          "MEDGEN:67439",
          "MESH:D056929",
          "MedDRA:10037113",
          "MedDRA:10052313",
          "NANDO:2100131",
          "NANDO:2200363",
          "NCIT:C84827",
          "NORD:2034",
          "OMIMPS:177200",
          "Orphanet:526",
          "SCTID:707747007",
          "UMLS:C0221043"
        ],
        "synonyms": [
          "Liddle syndrome",
          "pseudoaldosteronism",
          "pseudohyperaldosteronism type 1",
          "LIDLS"
        ],
        "categories": [
          {
            "ref": "MONDO:0002118",
            "name": "urinary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A rare genetic form of low-renin hypertension characterized by hypertension associated with decreased plasma levels of potassium and aldosterone."
      },
      "child_count": 9,
      "reference_id": "MONDO:0008323"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9629,
      "label": "Liddle syndrome"
    }
  ]
}