{
  "id": 16163,
  "label": "atrial standstill",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015281",
  "properties": {
    "xrefs": [
      "GARD:0016564",
      "ICD9:426.6",
      "MEDGEN:639047",
      "MESH:C563984",
      "Orphanet:1344",
      "SCTID:450919004",
      "UMLS:C0541782",
      "icd11.foundation:483869734"
    ],
    "synonyms": [
      "atrial cardiomyopathy with heart block"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Atrial standstill is a rare cardiac rhythm disease with a few familial and sporadic cases described to date that is characterized by a transient or permanent absence of electrical and mechanical atrial activity. Electrocardiographic findings include bradycardia, ectopic supraventricular rhythms, lack of atrial excitability and absent P waves."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6919,
        6933
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020532",
          "ICD9:425.4",
          "MEDGEN:468561",
          "OMIMPS:115210",
          "Orphanet:217635",
          "SCTID:233878008",
          "UMLS:C0340429"
        ],
        "synonyms": [
          "hereditary restrictive cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of restrictive cardiomyopathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 20,
      "reference_id": "MONDO:0016340"
    }
  ],
  "children": [
    {
      "id": 8578,
      "label": "atrial standstill 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16163
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080662",
          "GARD:0018611",
          "MEDGEN:1646392",
          "OMIM:108770",
          "UMLS:C4551959"
        ],
        "synonyms": [
          "atrial standstill 1",
          "atrial standstill type 1",
          "atrial standstill, digenic (GJA5/SCN5A)",
          "ATRST1",
          "atrial cardiomyopathy with heart block",
          "cardiomyopathy, familial, with conduction disturbance"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any atrial standstill in which the cause of the disease is a mutation in both the GJA5 and SCN5A genes."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007171"
    },
    {
      "id": 15332,
      "label": "atrial standstill 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16163
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080663",
          "GARD:0018612",
          "MEDGEN:816731",
          "OMIM:615745",
          "UMLS:C3810401"
        ],
        "synonyms": [
          "NPPA atrial standstill",
          "atrial standstill 2",
          "atrial standstill caused by mutation in NPPA",
          "atrial standstill type 2",
          "ATRST2",
          "atrial dilation and standstill",
          "cardiomyopathy, atrial dilated, with atrial standstill"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any atrial standstill in which the cause of the disease is a mutation in the NPPA gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014329"
    }
  ],
  "roots": [
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy"
    }
  ]
}