{
  "id": 16881,
  "label": "familial isolated arrhythmogenic right ventricular dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016342",
  "properties": {
    "xrefs": [
      "GARD:0017129",
      "MEDGEN:901869",
      "OMIMPS:107970",
      "Orphanet:217656",
      "SCTID:715865008",
      "UMLS:C4274968",
      "icd11.foundation:460188584"
    ],
    "synonyms": [
      "familial isolated ARVC",
      "familial isolated ARVD",
      "familial isolated arrhythmogenic right ventricular cardiomyopathy",
      "familial isolated arrhythmogenic right ventricular dysplasia",
      "familial isolated arrhythmogenic ventricular cardiomyopathy",
      "familial isolated arrhythmogenic ventricular dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Familial isolated arrhythmogenic right ventricular dysplasia (ARVC) is the familial autosomal dominant form of ARVC, a heart muscle disease characterized by life-threatening ventricular arrhythmias with left bundle branch block configuration that may manifest with palpitations, ventricular tachycardia, syncope and sudden fatal attacks, and that is due to dystrophy and fibro-fatty replacement of the right ventricular myocardium that may lead to right ventricular aneurysms."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 16,
  "parents": [
    {
      "id": 6933,
      "label": "familial cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6735,
        24272
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0002945",
          "GARD:0024166",
          "ICD9:425.4",
          "MEDGEN:538845",
          "SCTID:35728003",
          "UMLS:C0264789",
          "icd11.foundation:1018022925"
        ],
        "synonyms": [
          "hereditary cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An instance of cardiomyopathy that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 18,
      "reference_id": "MONDO:0005217"
    },
    {
      "id": 17077,
      "label": "arrhythmogenic right ventricular cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3007
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050431",
          "GARD:0005847",
          "ICD9:425.4",
          "MEDGEN:87618",
          "MESH:D019571",
          "MedDRA:10058093",
          "NANDO:2100055",
          "NANDO:2200230",
          "NCIT:C84571",
          "Orphanet:247",
          "SCTID:281170005",
          "UMLS:C0349788",
          "icd11.foundation:1931494126"
        ],
        "synonyms": [
          "ARVD",
          "arrhythmogenic RVD",
          "arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular dysplasia",
          "right ventricular dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that consists in progressive dystrophy of primarily the right ventricular myocardium with fibro-fatty replacement and ventricular dilation, and that is clinically characterized by ventricular arrhythmias and a risk of sudden cardiac death."
      },
      "child_count": 2,
      "reference_id": "MONDO:0016587"
    }
  ],
  "children": [
    {
      "id": 3181,
      "label": "arrhythmogenic right ventricular dysplasia 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110084",
          "GARD:0022844",
          "MEDGEN:816468",
          "OMIM:615616",
          "UMLS:C3810138"
        ],
        "synonyms": [
          "ARVC13",
          "ARVD13",
          "CTNNA3 arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular cardiomyopathy 13",
          "arrhythmogenic right ventricular cardiomyopathy caused by mutation in CTNNA3",
          "arrhythmogenic right ventricular dysplasia type 13",
          "arrhythmogenic right ventricular dysplasia, familial, 13",
          "arrhythmogenic right ventricular dysplasia, familial, type 13"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the CTNNA3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0000908"
    },
    {
      "id": 8559,
      "label": "arrhythmogenic right ventricular dysplasia 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110070",
          "GARD:0024526",
          "MEDGEN:349530",
          "OMIM:107970",
          "UMLS:C1862511"
        ],
        "synonyms": [
          "ARVC1",
          "ARVD1",
          "TGFB3 arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular cardiomyopathy 1",
          "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3",
          "arrhythmogenic right ventricular dysplasia type 1",
          "arrhythmogenic right ventricular dysplasia, familial, type 1",
          "familial arrhythmogenic right ventricular dysplasia 1",
          "Uhl anomaly",
          "arrhythmogenic right ventricular dysplasia, familial, 1",
          "cardiomyopathy, right ventricular dilated"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the TGFB3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007152"
    },
    {
      "id": 12310,
      "label": "arrhythmogenic right ventricular dysplasia 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110072",
          "GARD:0024780",
          "MEDGEN:356108",
          "MESH:C566584",
          "OMIM:602086",
          "UMLS:C1865882"
        ],
        "synonyms": [
          "ARVC3",
          "ARVD3",
          "arrhythmogenic right ventricular cardiomyopathy 3",
          "arrhythmogenic right ventricular dysplasia type 3",
          "arrhythmogenic right ventricular dysplasia, familial, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An arrhythmogenic right ventricular dysplasia associated with variation in the region 14q12-q22."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011188"
    },
    {
      "id": 12311,
      "label": "arrhythmogenic right ventricular dysplasia 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110073",
          "GARD:0024781",
          "MEDGEN:356107",
          "MESH:C566583",
          "OMIM:602087",
          "UMLS:C1865881"
        ],
        "synonyms": [
          "ARVC4",
          "ARVD4",
          "arrhythmogenic right ventricular cardiomyopathy 4",
          "arrhythmogenic right ventricular dysplasia type 4",
          "fanilial arrhythmogenic right ventricular dysplasia 4",
          "arrhythmogenic right ventricular dysplasia, familial, 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An arrhythmogenic right ventricular dysplasia associated with variation in the region 2q32.1-q32.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011189"
    },
    {
      "id": 12563,
      "label": "arrhythmogenic right ventricular dysplasia 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110074",
          "GARD:0024800",
          "MEDGEN:346805",
          "MESH:C565776",
          "OMIM:604400",
          "UMLS:C1858379"
        ],
        "synonyms": [
          "ARVC5",
          "ARVD5",
          "TMEM43 arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular cardiomyopathy 5",
          "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TMEM43",
          "arrhythmogenic right ventricular dysplasia 5",
          "arrhythmogenic right ventricular dysplasia type 5",
          "arrhythmogenic right ventricular dysplasia, familial, type 5",
          "arrhythmogenic right ventricular dysplasia, familial, 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the TMEM43 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011459"
    },
    {
      "id": 12564,
      "label": "arrhythmogenic right ventricular dysplasia 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110075",
          "GARD:0024801",
          "MEDGEN:346892",
          "MESH:C565775",
          "OMIM:604401",
          "UMLS:C1858378"
        ],
        "synonyms": [
          "ARVC6",
          "ARVD6",
          "arrhythmogenic right ventricular cardiomyopathy 6",
          "arrhythmogenic right ventricular dysplasia type 6",
          "arrhythmogenic right ventricular dysplasia, familial, 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An arrhythmogenic right ventricular dysplasia associated with variation in the region 10p14-p12."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011460"
    },
    {
      "id": 12586,
      "label": "catecholaminergic polymorphic ventricular tachycardia 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881,
        18166
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060675",
          "DOID:0110071",
          "GARD:0024803",
          "MEDGEN:351513",
          "MESH:C563409",
          "NCIT:C123414",
          "OMIM:600996",
          "OMIM:604772",
          "UMLS:C1631597"
        ],
        "synonyms": [
          "ARVC2",
          "ARVD2",
          "RYR2 familial isolated arrhythmogenic right ventricular dysplasia",
          "arrhythmogenic right ventricular cardiomyopathy 2",
          "arrhythmogenic right ventricular dysplasia 2",
          "arrhythmogenic right ventricular dysplasia type 2",
          "arrhythmogenic right ventricular dysplasia, familial, type 2",
          "catecholaminergic polymorphic ventricular tachycardia 1",
          "catecholaminergic polymorphic ventricular tachycardia type 1",
          "familial arrhythmogenic right ventricular dysplasia 2",
          "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2",
          "ventricular tachycardia, catecholaminergic polymorphic, 1",
          "CPVT1",
          "arrhythmogenic right ventricular dysplasia, familial, 2",
          "ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy",
          "ventricular tachycardia, stress-induced polymorphic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Polymorphic ventricular tachycardia induced by adrenergic stress. It is inherited in an autosomal dominant pattern and is caused by mutations in the ryanodine receptor 2 (RYR2) gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011484"
    },
    {
      "id": 12912,
      "label": "arrhythmogenic right ventricular dysplasia 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110076",
          "GARD:0024825",
          "MEDGEN:336069",
          "MESH:C564400",
          "OMIM:607450",
          "UMLS:C1843896"
        ],
        "synonyms": [
          "ARVC8",
          "ARVD8",
          "DSP arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular cardiomyopathy 8",
          "arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSP",
          "arrhythmogenic right ventricular dysplasia 8",
          "arrhythmogenic right ventricular dysplasia type 8",
          "arrhythmogenic right ventricular dysplasia, familial, type 8",
          "arrhythmogenic right ventricular dysplasia, familial, 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the DSP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011831"
    },
    {
      "id": 13243,
      "label": "arrhythmogenic right ventricular dysplasia 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110077",
          "GARD:0024852",
          "MEDGEN:373205",
          "MESH:C563808",
          "OMIM:609040",
          "UMLS:C1836906"
        ],
        "synonyms": [
          "ARVC9",
          "ARVD9",
          "PKP2 familial isolated arrhythmogenic right ventricular dysplasia",
          "arrhythmogenic right ventricular cardiomyopathy 9",
          "arrhythmogenic right ventricular dysplasia 9",
          "arrhythmogenic right ventricular dysplasia type 9",
          "arrhythmogenic right ventricular dysplasia, familial, type 9",
          "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in PKP2",
          "arrhythmogenic right ventricular dysplasia, familial, 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the PKP2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012180"
    },
    {
      "id": 13484,
      "label": "arrhythmogenic right ventricular dysplasia 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110081",
          "GARD:0024865",
          "MEDGEN:347543",
          "MESH:C565707",
          "OMIM:610193",
          "UMLS:C1857777"
        ],
        "synonyms": [
          "ARVC10",
          "ARVD10",
          "DSG2 arrhythmogenic right ventricular cardiomyopathy",
          "arrhythmogenic right ventricular cardiomyopathy 10",
          "arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSG2",
          "arrhythmogenic right ventricular dysplasia 10",
          "arrhythmogenic right ventricular dysplasia type 10",
          "arrhythmogenic right ventricular dysplasia, familial, type 10",
          "arrhythmogenic right ventricular dysplasia, familial, 10"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any arrhythmogenic right ventricular cardiomyopathy in which the cause of the disease is a mutation in the DSG2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012434"
    },
    {
      "id": 13554,
      "label": "arrhythmogenic right ventricular dysplasia 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110082",
          "GARD:0024870",
          "MEDGEN:351237",
          "MESH:C566471",
          "OMIM:610476",
          "UMLS:C1864850"
        ],
        "synonyms": [
          "ARVC11",
          "ARVD11",
          "DSC2 familial isolated arrhythmogenic right ventricular dysplasia",
          "arrhythmogenic right ventricular cardiomyopathy 11",
          "arrhythmogenic right ventricular dysplasia 11",
          "arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair",
          "arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and wooly hair",
          "arrhythmogenic right ventricular dysplasia type 11",
          "arrhythmogenic right ventricular dysplasia, familial, type 11",
          "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in DSC2",
          "arrhythmogenic right ventricular dysplasia, familial, 11",
          "arrhythmogenic right ventricular dysplasia, familial, 11, and mild palmoplantar keratoderma with or without woolly hair",
          "arrhythmogenic right ventricular dysplasia, familial, 11, and mild palmoplantar keratoderma with or without wooly hair",
          "arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair",
          "arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and wooly hair"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the DSC2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012506"
    },
    {
      "id": 13724,
      "label": "arrhythmogenic right ventricular dysplasia 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110083",
          "GARD:0024880",
          "MEDGEN:409749",
          "MESH:C566925",
          "OMIM:611528",
          "UMLS:C1969081"
        ],
        "synonyms": [
          "ARVC12",
          "ARVD12",
          "JUP familial isolated arrhythmogenic right ventricular dysplasia",
          "arrhythmogenic right ventricular cardiomyopathy 12",
          "arrhythmogenic right ventricular dysplasia 12",
          "arrhythmogenic right ventricular dysplasia type 12",
          "arrhythmogenic right ventricular dysplasia, familial, type 12",
          "familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in JUP",
          "arrhythmogenic right ventricular dysplasia, familial, 12"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any familial isolated arrhythmogenic right ventricular dysplasia in which the cause of the disease is a mutation in the JUP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012684"
    },
    {
      "id": 17708,
      "label": "familial isolated arrhythmogenic ventricular dysplasia, left dominant form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070534",
          "GARD:0017345",
          "MEDGEN:1863454",
          "Orphanet:293888",
          "UMLS:C5925017"
        ],
        "synonyms": [
          "familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017401"
    },
    {
      "id": 17709,
      "label": "familial isolated arrhythmogenic ventricular dysplasia, biventricular form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070535",
          "GARD:0017346",
          "MEDGEN:1864265",
          "Orphanet:293899",
          "UMLS:C5925016"
        ],
        "synonyms": [
          "familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017402"
    },
    {
      "id": 17710,
      "label": "familial isolated arrhythmogenic ventricular dysplasia, right dominant form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017347",
          "MEDGEN:1864032",
          "Orphanet:293910",
          "UMLS:C5925015"
        ],
        "synonyms": [
          "familial isolated arrhythmogenic ventricular cardiomyopathy, classic form",
          "familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form",
          "familial isolated arrhythmogenic ventricular dysplasia, classic form"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017403"
    },
    {
      "id": 21838,
      "label": "arrhythmogenic right ventricular dysplasia, familial, 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16881
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080959",
          "GARD:0025519",
          "MEDGEN:1712001",
          "OMIM:618920",
          "UMLS:C5394505"
        ],
        "synonyms": [
          "ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14",
          "ARVD14",
          "Arrhythmogenic Right Ventricular Cardiomyopathy 14",
          "arrhythmogenic right ventricular dysplasia, familial, 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030062"
    }
  ],
  "roots": [
    {
      "id": 6933,
      "label": "familial cardiomyopathy"
    },
    {
      "id": 17077,
      "label": "arrhythmogenic right ventricular cardiomyopathy"
    }
  ]
}