{
  "id": 19268,
  "label": "ATTRV122I amyloidosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019441",
  "properties": {
    "xrefs": [
      "GARD:0016755",
      "MEDGEN:907865",
      "Orphanet:85451",
      "SCTID:715655000",
      "UMLS:C4275067",
      "icd11.foundation:1449168185"
    ],
    "synonyms": [
      "ATTRV122I-related amyloidosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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"
    },
    {
      "id": 26000,
      "label": "amyloidosis, hereditary systemic 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8513
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027098",
          "MEDGEN:414031",
          "OMIM:105210",
          "UMLS:C2751492"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0971004"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16880,
      "label": "familial restrictive cardiomyopathy"
    },
    {
      "id": 26000,
      "label": "amyloidosis, hereditary systemic 1"
    }
  ]
}