{
  "id": 18192,
  "label": "wild type ATTR amyloidosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018018",
  "properties": {
    "xrefs": [
      "DOID:0080937",
      "GARD:0021501",
      "ICD10CM:E85.82",
      "ICD9:277.39",
      "MEDGEN:87446",
      "NANDO:1200212",
      "Orphanet:330001",
      "SCTID:237877004",
      "UMLS:C0342623",
      "icd11.foundation:25699053"
    ],
    "synonyms": [
      "ATTRwt amyloidosis",
      "ATTRwt-related amyloidosis",
      "SSA",
      "Senile systemic amyloidosis",
      "wild type ATTR-related amyloidosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16883,
      "label": "non-familial restrictive cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6919
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020535",
          "MEDGEN:1843079",
          "NANDO:1200294",
          "Orphanet:217720",
          "UMLS:C5680885",
          "icd11.foundation:2097520643"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0016345"
    },
    {
      "id": 18960,
      "label": "amyloidosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20409
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9120",
          "EFO:1001875",
          "GARD:0018676",
          "HP:0011034",
          "ICD10CM:E85",
          "ICD10WHO:E85",
          "ICD9:277.3",
          "ICD9:277.30",
          "MEDGEN:272",
          "MESH:D000686",
          "MedDRA:10002022",
          "NANDO:2200138",
          "NCIT:C2868",
          "ONCOTREE:MIDDA",
          "Orphanet:69",
          "SCTID:17602002",
          "UMLS:C0002726",
          "icd11.foundation:2078467774"
        ],
        "synonyms": [
          "amyloid",
          "amyloid disease",
          "amyloidoses",
          "amyloidosis",
          "amyloidosis (disease)"
        ],
        "definition": "A disorder characterized by the localized or diffuse accumulation of amyloid protein in various anatomic sites. It may be primary, due to clonal plasma cell proliferations; secondary, due to long standing infections, chronic inflammatory disorders, or malignancies; or familial. It may affect the nerves, skin, tongue, joints, heart, liver, spleen, kidneys and adrenal glands."
      },
      "child_count": 12,
      "reference_id": "MONDO:0019065"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16883,
      "label": "non-familial restrictive cardiomyopathy"
    },
    {
      "id": 18960,
      "label": "amyloidosis"
    }
  ]
}