{
  "id": 21518,
  "label": "familial hypertrophic cardiomyopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024573",
  "properties": {
    "xrefs": [
      "DOID:0080326",
      "MEDGEN:183649",
      "MESH:D024741",
      "NCIT:C84773",
      "OMIMPS:192600",
      "Orphanet:155",
      "SCTID:471885006",
      "UMLS:C0949658",
      "icd11.foundation:1408928442"
    ],
    "synonyms": [
      "cardiomyopathy, familial hypertrophic",
      "familial hypertrophic cardiomyopathy",
      "familila or idiopathic hypertrophic obstructive cardiomyopathy",
      "hereditary hypertrophic cardiomyopathy",
      "hypertrophic familial cardiomyopathy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      }
    ],
    "definition": "Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 40,
  "parents": [
    {
      "id": 6777,
      "label": "hypertrophic cardiomyopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3007
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11984",
          "EFO:0000538",
          "HP:0001639",
          "ICD10CM:I42.1",
          "ICD10CM:I42.2",
          "ICD9:425.1",
          "ICD9:425.11",
          "ICD9:425.4",
          "MEDGEN:2881",
          "MESH:D002312",
          "MedDRA:10020871",
          "NANDO:1200286",
          "NANDO:1200288",
          "NANDO:2100054",
          "NANDO:2200229",
          "NANDO:2201042",
          "NCIT:C34449",
          "Orphanet:217569",
          "SCTID:233873004",
          "UMLS:C0007194",
          "icd11.foundation:1830681485"
        ],
        "synonyms": [
          "hypertrophic cardiomyopathy",
          "hypertrophic subaortic stenosis",
          "obstructive hypertrophic cardiomyopathy",
          "familial hypertrophic cardiomyopathy",
          "HCM - hypertrophic cardiomyopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A condition in which the myocardium is hypertrophied without an obvious cause. The hypertrophy is generally asymmetric and may be associated with obstruction of the ventricular outflow tract."
      },
      "child_count": 3,
      "reference_id": "MONDO:0005045"
    },
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 8668,
      "label": "hypertrophic cardiomyopathy 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518,
        26612
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110308",
          "GARD:0024540",
          "MEDGEN:349383",
          "MESH:C566171",
          "NCIT:C142892",
          "OMIM:115195",
          "UMLS:C1861864"
        ],
        "synonyms": [
          "CMH2",
          "TNNT2 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 2",
          "cardiomyopathy, hypertrophic, 2",
          "familial hypertrophic cardiomyopathy type 2",
          "hypertrophic cardiomyopathy 2",
          "hypertrophic cardiomyopathy caused by mutation in TNNT2",
          "hypertrophic cardiomyopathy type 2",
          "cardiomyopathy, familial hypertrophic, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007266"
    },
    {
      "id": 8669,
      "label": "hypertrophic cardiomyopathy 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110309",
          "GARD:0024541",
          "MEDGEN:349382",
          "MESH:C566170",
          "OMIM:115196",
          "UMLS:C1861863"
        ],
        "synonyms": [
          "CMH3",
          "TPM1 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 3",
          "cardiomyopathy, hypertrophic, 3",
          "hypertrophic cardiomyopathy 3",
          "hypertrophic cardiomyopathy caused by mutation in TPM1",
          "hypertrophic cardiomyopathy type 3",
          "cardiomyopathy, familial hypertrophic, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TPM1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007267"
    },
    {
      "id": 8670,
      "label": "hypertrophic cardiomyopathy 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110310",
          "GARD:0024542",
          "MEDGEN:350526",
          "MESH:C566169",
          "NCIT:C133725",
          "OMIM:115197",
          "UMLS:C1861862"
        ],
        "synonyms": [
          "CMH4",
          "MYBPC3 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, 4",
          "cardiomyopathy, familial hypertrophic, type 4",
          "cardiomyopathy, hypertrophic, 4",
          "familial hypertrophic cardiomyopathy type 4",
          "hypertrophic cardiomyopathy 4",
          "hypertrophic cardiomyopathy caused by mutation in MYBPC3",
          "hypertrophic cardiomyopathy type 4",
          "cardiomyopathy, familial hypertrophic, 4, susceptibility to"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An autosomal dominant condition caused by mutation(s) in the MYBPC3 gene, encoding MYBPC3 protein. It is characterized by severe neonatal hypertrophic cardiomyopathy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007268"
    },
    {
      "id": 8915,
      "label": "Beckwith-Wiedemann syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16218,
        19480,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:5572",
          "GARD:0003343",
          "ICD9:759.89",
          "MEDGEN:2562",
          "MESH:D001506",
          "MedDRA:10050344",
          "NANDO:2200959",
          "NCIT:C34415",
          "NORD:845",
          "OMIM:130650",
          "Orphanet:116",
          "SCTID:81780002",
          "UMLS:C0004903",
          "icd11.foundation:803086260"
        ],
        "synonyms": [
          "BWS",
          "Beckwith-Wiedemann syndrome",
          "Wiedemann-Beckwith syndrome",
          "exomphalos-macroglossia-gigantism syndrome",
          "Beckwith-Wiedemann syndrome chromosome region",
          "EMG syndrome",
          "Wiedemann-Beckwith syndrome (WBS)",
          "exomphalos macroglossia gigantism syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Beckwith-Wiedemann syndrome (BWS) is a genetic disorder characterized by overgrowth, tumor predisposition and congenital malformations."
      },
      "child_count": 24,
      "reference_id": "MONDO:0007534"
    },
    {
      "id": 9379,
      "label": "myotonic dystrophy type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16733,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11722",
          "GARD:0008310",
          "ICD9:359.21",
          "MEDGEN:886881",
          "NCIT:C84679",
          "NORD:1075",
          "OMIM:160900",
          "Orphanet:273",
          "UMLS:C3250443",
          "icd11.foundation:557405480"
        ],
        "synonyms": [
          "DM1",
          "DMPK myotonic dystrophy",
          "MD1",
          "Myotonic Dystrophy",
          "Steinert disease",
          "Steinert myotonic dystrophy syndrome",
          "Steinert syndrome",
          "dystrophia myotonica",
          "myotonic dystrophy caused by mutation in DMPK",
          "myotonic dystrophy type 1",
          "Steinert myotonic dystrophy",
          "Steinert's disease",
          "dystrophia myotonica 1",
          "dystrophia myotonica type 1",
          "myotonic dystrophy 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Steinert disease, also known as myotonic dystrophy type 1, is a muscle disease characterized by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008056"
    },
    {
      "id": 9928,
      "label": "hypertrophic cardiomyopathy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110307",
          "GARD:0024636",
          "MEDGEN:501195",
          "OMIM:192600",
          "UMLS:C3495498"
        ],
        "synonyms": [
          "CMH1",
          "MYH7 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant",
          "cardiomyopathy, familial hypertrophic, type 1",
          "cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant",
          "cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant",
          "hypertrophic cardiomyopathy 1",
          "hypertrophic cardiomyopathy caused by mutation in MYH7",
          "hypertrophic cardiomyopathy type 1",
          "Cmh",
          "asymmetric septal Hypertrophy",
          "cardiomyopathy, familial hypertrophic, 1",
          "hypertrophic subaortic stenosis, idiopathic",
          "ventricular Hypertrophy, hereditary"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008647"
    },
    {
      "id": 9996,
      "label": "very long chain acyl-CoA dehydrogenase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17948,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080155",
          "GARD:0005508",
          "ICD10CM:E71.310",
          "MEDGEN:854382",
          "NANDO:2200512",
          "NANDO:2201139",
          "NCIT:C98647",
          "NORD:1827",
          "OMIM:201475",
          "Orphanet:26793",
          "SCTID:237997005",
          "UMLS:C3887523",
          "icd11.foundation:907810567"
        ],
        "synonyms": [
          "VLCAD",
          "VLCAD deficiency",
          "VLCADD",
          "Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD)",
          "acyl-CoA dehydrogenase, very long-chain deficiency",
          "very long chain acyl-CoA dehydrogenase deficiency",
          "very long-chain acyl-CoA dehydrogenase deficiency",
          "very long-chain acyl-Coenzyme A dehydrogenase deficiency",
          "ACADVLD",
          "acyl-CoA dehydrogenase, very long-chain, deficiency OF"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "An inherited disorder of mitochondrial long-chain fatty acid oxidation with a variable presentation including: cardiomyopathy, hypoketotic hypoglycemia, liver disease, exercise intolerance and rhabdomyolysis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008723"
    },
    {
      "id": 10522,
      "label": "multiple acyl-CoA dehydrogenase deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2735,
        5908,
        17949,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060358",
          "GARD:0006523",
          "ICD10CM:E71.313",
          "MEDGEN:75696",
          "NANDO:1200801",
          "NANDO:2200502",
          "NCIT:C84907",
          "NORD:1192",
          "OMIM:231680",
          "Orphanet:26791",
          "UMLS:C0268596",
          "icd11.foundation:977130875"
        ],
        "synonyms": [
          "Glutaric Aciduria Type II",
          "MAD deficiency",
          "MADD",
          "electron transfer flavoprotein deficiency",
          "glutaric acidemia type 2",
          "glutaric acidemia type II",
          "glutaric aciduria type 2",
          "glutaric aciduria, type 2",
          "multiple acyl Coenzyme A dehydrogenase deficiency",
          "multiple acyl-CoA dehydrogenase deficiency",
          "Etfa deficiency",
          "Etfb deficiency",
          "Etfdh deficiency",
          "glutaric acidemia 2A",
          "glutaric acidemia 2B",
          "glutaric acidemia 2C",
          "glutaric acidemia IIA",
          "glutaric acidemia IIB",
          "glutaric acidemia IIC",
          "EMA",
          "Ga 2",
          "ethylmalonic-Adipicaciduria",
          "glutaric acidemia 2",
          "glutaric aciduria 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A disorder of fatty acid and amino acid oxidation, caused by mutations in ETFDH, ETFA, or ETFB, and is a clinically heterogeneous disorder ranging from a severe neonatal presentation with metabolic acidosis, cardiomyopathy and liver disease, to a mild childhood/adult disease with episodic metabolic decompensation, muscle weakness, and respiratory failure."
      },
      "child_count": 20,
      "reference_id": "MONDO:0009282"
    },
    {
      "id": 11904,
      "label": "46,XY complete gonadal dysgenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4130,
        20383,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14448",
          "GARD:0005068",
          "MEDGEN:445380",
          "MESH:D006061",
          "NCIT:C120198",
          "NORD:1750",
          "OMIMPS:400044",
          "Orphanet:242",
          "SCTID:95218005",
          "UMLS:C2936694"
        ],
        "synonyms": [
          "46 XY gonadal dysgenesis",
          "46, XY CGD",
          "46, XY complete gonadal dysgenesis",
          "46, XY pure gonadal dysgenesis",
          "46,XY CGD",
          "46,XY SEX reversal",
          "46,XY gonadal dysgenesis",
          "46,XY pure gonadal dysgenesis",
          "Swyer syndrome",
          "gonadal dysgenesis, XY female type",
          "sex-reversing locus on X",
          "sex-reversing locus on X, formerly",
          "testis-determining Factor, X-chromosomal"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "46,XY complete gonadal dysgenesis (46,XY CGD) is a disorder of sex development (DSD) associated with anomalies in gonadal development that result in the presence of female external and internal genitalia despite the 46,XY karyotype."
      },
      "child_count": 36,
      "reference_id": "MONDO:0010765"
    },
    {
      "id": 12076,
      "label": "hypertrophic cardiomyopathy 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518,
        25068
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110312",
          "GARD:0024763",
          "MEDGEN:331466",
          "MESH:C563436",
          "OMIM:600858",
          "UMLS:C1833236"
        ],
        "synonyms": [
          "CMH6",
          "PRKAG2 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 6",
          "cardiomyopathy, hypertrophic 6",
          "hypertrophic cardiomyopathy 6",
          "hypertrophic cardiomyopathy caused by mutation in PRKAG2",
          "hypertrophic cardiomyopathy type 6",
          "cardiomyopathy, familial hypertrophic, 6"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the PRKAG2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010946"
    },
    {
      "id": 12220,
      "label": "dilated cardiomyopathy 1C",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18829,
        21518,
        24709
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110423",
          "GARD:0015331",
          "MEDGEN:316944",
          "MESH:C563307",
          "NCIT:C170436",
          "OMIM:601493",
          "UMLS:C1832244"
        ],
        "synonyms": [
          "cardiomyopathy, dilated, 1C, with or without LVNC",
          "cardiomyopathy, hypertrophic, 24",
          "dilated cardiomyopathy type 1C",
          "CMD1C",
          "cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction",
          "cardiomyopathy, familial hypertrophic, 24",
          "left ventricular noncompaction 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A dilated cardiomyopathy that has material basis in mutation in the LDB3 gene on chromosome 10q23.2."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011094"
    },
    {
      "id": 12924,
      "label": "hypertrophic cardiomyopathy 25",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16779,
        16878,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110328",
          "GARD:0024827",
          "MEDGEN:895360",
          "MESH:C564388",
          "OMIM:607487",
          "UMLS:C4225408"
        ],
        "synonyms": [
          "CMH25",
          "TCAP hypertrophic cardiomyopathy",
          "Tcap hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 25",
          "cardiomyopathy, hypertrophic, 25",
          "hypertrophic cardiomyopathy caused by mutation in TCAP",
          "hypertrophic cardiomyopathy type 25",
          "cardiomyopathy, familial hypertrophic, 25"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011843"
    },
    {
      "id": 13177,
      "label": "hypertrophic cardiomyopathy 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110314",
          "GARD:0024842",
          "MEDGEN:324806",
          "MESH:C563866",
          "OMIM:608751",
          "UMLS:C1837471"
        ],
        "synonyms": [
          "MYL3 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, 8",
          "cardiomyopathy, familial hypertrophic, type 8",
          "cardiomyopathy, hypertrophic, 8",
          "hypertrophic cardiomyopathy 8",
          "hypertrophic cardiomyopathy caused by mutation in MYL3",
          "hypertrophic cardiomyopathy type 8",
          "CMH8",
          "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012111"
    },
    {
      "id": 13178,
      "label": "hypertrophic cardiomyopathy 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110316",
          "GARD:0024843",
          "MEDGEN:331754",
          "MESH:C563865",
          "OMIM:608758",
          "UMLS:C1834460"
        ],
        "synonyms": [
          "CMH10",
          "MYL2 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, 10",
          "cardiomyopathy, familial hypertrophic, type 10",
          "cardiomyopathy, hypertrophic, 10",
          "hypertrophic cardiomyopathy 10",
          "hypertrophic cardiomyopathy caused by mutation in MYL2",
          "hypertrophic cardiomyopathy type 10",
          "cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012112"
    },
    {
      "id": 13236,
      "label": "long chain 3-hydroxyacyl-CoA dehydrogenase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17948,
        19748,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0061186",
          "GARD:0006867",
          "MEDGEN:778253",
          "NCIT:C129929",
          "OMIM:609016",
          "Orphanet:5",
          "SCTID:726021008",
          "UMLS:C3711645",
          "icd11.foundation:760613381"
        ],
        "synonyms": [
          "HELLP syndrome, maternal, of pregnancy",
          "LCHAD deficiency",
          "LCHADD",
          "fatty liver, acute, of pregnancy",
          "long chain 3-hydroxyacyl-CoA dehydrogenase deficiency",
          "long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency",
          "3-hydroxyacyl-CoA dehydrogenase long chain deficiency",
          "long-chain 3-OH acyl-CoA dehydrogenase deficiency",
          "long-chain 3-hydroxy acyl CoA dehydrogenase deficiency",
          "long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency",
          "trifunctional protein deficiency type 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood with hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and frequently cardiac involvement with arrhythmias and/or cardiomyopathy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012173"
    },
    {
      "id": 13605,
      "label": "cardiomyopathy-hypotonia-lactic acidosis syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        7626,
        17234,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016795",
          "MEDGEN:324373",
          "MESH:C563665",
          "OMIM:610773",
          "Orphanet:91130",
          "SCTID:718713000",
          "UMLS:C1835845"
        ],
        "synonyms": [
          "hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome",
          "Mpcd",
          "mitochondrial phosphate carrier deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Cardiomyopathy-hypotonia-lactic acidosis syndrome is characterized by hypertrophic cardiomyopathy, muscular hypotonia and the presence of lactic acidosis at birth. It has been described in two sisters (both of whom died within the first year of life) from a nonconsanguineous Turkish family. The syndrome is caused by a homozygous point mutation in the exon 3A of the SLC25A3 gene encoding a mitochondrial membrane transporter."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012557"
    },
    {
      "id": 13839,
      "label": "hypertrophic cardiomyopathy 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110317",
          "GARD:0024889",
          "MEDGEN:436962",
          "MESH:C567419",
          "OMIM:612098",
          "UMLS:C2677506"
        ],
        "synonyms": [
          "ACTC1 hypertrophic cardiomyopathy",
          "CMH11",
          "cardiomyopathy, familial hypertrophic, type 11",
          "cardiomyopathy, hypertrophic, 11",
          "hypertrophic cardiomyopathy 11",
          "hypertrophic cardiomyopathy caused by mutation in ACTC1",
          "hypertrophic cardiomyopathy type 11",
          "cardiomyopathy, familial hypertrophic, 11"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the ACTC1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012799"
    },
    {
      "id": 13844,
      "label": "hypertrophic cardiomyopathy 12",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110318",
          "GARD:0024890",
          "MEDGEN:393755",
          "OMIM:612124",
          "UMLS:C2677491"
        ],
        "synonyms": [
          "CMH12",
          "CSRP3 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 12",
          "cardiomyopathy, hypertrophic, 12",
          "hypertrophic cardiomyopathy 12",
          "hypertrophic cardiomyopathy caused by mutation in CSRP3",
          "hypertrophic cardiomyopathy type 12",
          "cardiomyopathy, familial hypertrophic, 12"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012804"
    },
    {
      "id": 14231,
      "label": "hypertrophic cardiomyopathy 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110319",
          "GARD:0024906",
          "MEDGEN:442487",
          "MESH:C567686",
          "OMIM:613243",
          "UMLS:C2750472"
        ],
        "synonyms": [
          "CMH13",
          "TNNC1 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 13",
          "cardiomyopathy, hypertrophic, 13",
          "hypertrophic cardiomyopathy caused by mutation in TNNC1",
          "hypertrophic cardiomyopathy type 13",
          "cardiomyopathy, familial hypertrophic, 13"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNC1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013195"
    },
    {
      "id": 14233,
      "label": "hypertrophic cardiomyopathy 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110320",
          "GARD:0024907",
          "MEDGEN:442484",
          "MESH:C567684",
          "OMIM:613251",
          "UMLS:C2750467"
        ],
        "synonyms": [
          "CMH14",
          "MYH6 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 14",
          "cardiomyopathy, hypertrophic, 14",
          "hypertrophic cardiomyopathy caused by mutation in MYH6",
          "hypertrophic cardiomyopathy type 14",
          "cardiomyopathy, familial hypertrophic, 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYH6 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013197"
    },
    {
      "id": 14236,
      "label": "hypertrophic cardiomyopathy 15",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110321",
          "GARD:0024908",
          "MEDGEN:413312",
          "MESH:C567681",
          "OMIM:613255",
          "UMLS:C2750459"
        ],
        "synonyms": [
          "CMH15",
          "VCL hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 15",
          "cardiomyopathy, hypertrophic, 15",
          "hypertrophic cardiomyopathy caused by mutation in VCL",
          "hypertrophic cardiomyopathy type 15",
          "cardiomyopathy, familial hypertrophic, 15"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the VCL gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013200"
    },
    {
      "id": 14402,
      "label": "hypertrophic cardiomyopathy 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110313",
          "GARD:0024916",
          "MEDGEN:348695",
          "OMIM:613690",
          "UMLS:C1860752"
        ],
        "synonyms": [
          "CMH7",
          "TNNI3 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 7",
          "cardiomyopathy, hypertrophic, 7",
          "hypertrophic cardiomyopathy 7",
          "hypertrophic cardiomyopathy caused by mutation in TNNI3",
          "hypertrophic cardiomyopathy type 7",
          "cardiomyopathy, familial hypertrophic, 7"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013369"
    },
    {
      "id": 14444,
      "label": "hypertrophic cardiomyopathy 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518,
        24220
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110315",
          "GARD:0024921",
          "MEDGEN:348780",
          "MESH:C566044",
          "OMIM:613765",
          "UMLS:C1861065"
        ],
        "synonyms": [
          "CMH9",
          "TTN hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, 9",
          "cardiomyopathy, familial hypertrophic, type 9",
          "hypertrophic cardiomyopathy caused by mutation in TTN",
          "hypertrophic cardiomyopathy type 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TTN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013412"
    },
    {
      "id": 14486,
      "label": "hypertrophic cardiomyopathy 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110322",
          "GARD:0024927",
          "MEDGEN:462554",
          "OMIM:613838",
          "UMLS:C3151204"
        ],
        "synonyms": [
          "CMH16",
          "MYOZ2 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 16",
          "cardiomyopathy, hypertrophic, 16",
          "hypertrophic cardiomyopathy caused by mutation in MYOZ2",
          "hypertrophic cardiomyopathy type 16",
          "cardiomyopathy, familial hypertrophic, 16"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYOZ2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013455"
    },
    {
      "id": 14505,
      "label": "hypertrophic cardiomyopathy 17",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110323",
          "GARD:0024929",
          "MEDGEN:462614",
          "OMIM:613873",
          "UMLS:C3151264"
        ],
        "synonyms": [
          "CMH17",
          "JPH2 hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 17",
          "cardiomyopathy, hypertrophic, 17",
          "hypertrophic cardiomyopathy caused by mutation in JPH2",
          "hypertrophic cardiomyopathy type 17",
          "cardiomyopathy, familial hypertrophic, 17"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the JPH2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013474"
    },
    {
      "id": 14506,
      "label": "hypertrophic cardiomyopathy 18",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110324",
          "GARD:0024930",
          "MEDGEN:462615",
          "OMIM:613874",
          "UMLS:C3151265"
        ],
        "synonyms": [
          "CMH18",
          "PLN hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 18",
          "cardiomyopathy, hypertrophic, 18",
          "hypertrophic cardiomyopathy caused by mutation in PLN",
          "hypertrophic cardiomyopathy type 18",
          "cardiomyopathy, familial hypertrophic, 18"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the PLN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013475"
    },
    {
      "id": 14507,
      "label": "hypertrophic cardiomyopathy 19",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110325",
          "GARD:0024931",
          "OMIM:613875"
        ],
        "synonyms": [
          "CALR3 hypertrophic cardiomyopathy",
          "CMH19",
          "cardiomyopathy familial hypertrophic 19",
          "cardiomyopathy, familial hypertrophic, type 19",
          "hypertrophic cardiomyopathy caused by mutation in CALR3",
          "hypertrophic cardiomyopathy type 19",
          "cardiomyopathy, familial hypertrophic, 19"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CALR3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013476"
    },
    {
      "id": 14508,
      "label": "hypertrophic cardiomyopathy 20",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110326",
          "GARD:0024932",
          "MEDGEN:462617",
          "OMIM:613876",
          "UMLS:C3151267"
        ],
        "synonyms": [
          "CMH20",
          "NEXN hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, type 20",
          "cardiomyopathy, hypertrophic, 20",
          "hypertrophic cardiomyopathy caused by mutation in NEXN",
          "hypertrophic cardiomyopathy type 20",
          "cardiomyopathy, familial hypertrophic, 20"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the NEXN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013477"
    },
    {
      "id": 14865,
      "label": "hypertrophic cardiomyopathy 21",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110311",
          "GARD:0024956",
          "MEDGEN:766356",
          "OMIM:614676",
          "UMLS:C3553442"
        ],
        "synonyms": [
          "CMH21",
          "cardiomyopathy, hypertrophic, 21",
          "hypertrophic cardiomyopathy type 21",
          "cardiomyopathy, familial hypertrophic, 21"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A hypertrophic cardiomyopathy associated that has material basis in region 7p12.1-q21 variation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013852"
    },
    {
      "id": 15109,
      "label": "dilated cardiomyopathy 1KK",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16880,
        21518,
        24709
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110445",
          "GARD:0015926",
          "MEDGEN:811544",
          "OMIM:615248",
          "UMLS:C3714995"
        ],
        "synonyms": [
          "CMD1KK",
          "MYPN dilated cardiomyopathy",
          "cardiomyopathy, dilated, type 1Kk",
          "cardiomyopathy, hypertrophic, 22",
          "dilated cardiomyopathy caused by mutation in MYPN",
          "dilated cardiomyopathy type 1KK",
          "cardiomyopathy, dilated, 1KK",
          "cardiomyopathy, familial hypertrophic, 22",
          "cardiomyopathy, familial restrictive, 4"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any dilated cardiomyopathy in which the cause of the disease is a mutation in the MYPN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014100"
    },
    {
      "id": 15864,
      "label": "hypertrophic cardiomyopathy 26",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110327",
          "GARD:0025029",
          "MEDGEN:934716",
          "OMIM:617047",
          "UMLS:C4310749"
        ],
        "synonyms": [
          "CMH26",
          "FLNC hypertrophic cardiomyopathy",
          "cardiomyopathy, familial hypertrophic, 26",
          "cardiomyopathy, familial hypertrophic, type 26",
          "cardiomyopathy, familial restrictive 5",
          "hypertrophic cardiomyopathy caused by mutation in FLNC",
          "hypertrophic cardiomyopathy type 26",
          "cardiomyopathy, familial restrictive, 5"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the FLNC gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014883"
    },
    {
      "id": 19780,
      "label": "Noonan syndrome and Noonan-related syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20302,
        20383,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019561",
          "MEDGEN:1826127",
          "MESH:C537846",
          "Orphanet:98733",
          "UMLS:C5681679"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0020297"
    },
    {
      "id": 19978,
      "label": "long chain acyl-CoA dehydrogenase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17948,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009700",
          "MEDGEN:65087",
          "MESH:C535690",
          "NCIT:C84537",
          "Orphanet:99900",
          "SCTID:237996001",
          "UMLS:C0220711",
          "icd11.foundation:692829041"
        ],
        "synonyms": [
          "LCAD",
          "acyl-CoA dehydrogenase, long-chain deficiency",
          "inborn error of long-chain-acyl-CoA dehydrogenase activity",
          "inborn long-chain-acyl-CoA dehydrogenase activity disorder",
          "long chain acyl-CoA dehydrogenase deficiency",
          "long-chain acyl-CoA dehydrogenase deficiency",
          "long-chain acyl-Coenzyme A dehydrogenase deficiency",
          "rare inborn error of long-chain-acyl-CoA dehydrogenase activity",
          "ACADL deficiency",
          "LCAD deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ],
        "definition": "A genetic disorder characterized by deficiency of the enzyme long-chain acyl-coenzyme A dehydrogenase that metabolizes long-chain fatty acids. Signs and symptoms appear in infancy or childhood and may be triggered during fasting, illness or exercise. They include hypoglycemia, muscle weakness and lethargy."
      },
      "child_count": 0,
      "reference_id": "MONDO:0020531"
    },
    {
      "id": 21881,
      "label": "cardiomyopathy, familial hypertrophic, 28",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025536",
          "MEDGEN:1779612",
          "OMIM:619402",
          "UMLS:C5543616"
        ],
        "synonyms": [
          "CMH28",
          "cardiomyopathy, familial hypertrophic, 28"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030317"
    },
    {
      "id": 23640,
      "label": "cardiomyopathy, familial hypertrophic 27",
      "isLeaf": true,
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            "ref": "MONDO:0002081",
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          {
            "ref": "MONDO:0004995",
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          }
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          {
            "ref": "MONDO:0004995",
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          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800371"
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    {
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      ],
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      "reference_id": "MONDO:0979573"
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  "roots": [
    {
      "id": 6777,
      "label": "hypertrophic cardiomyopathy"
    },
    {
      "id": 6933,
      "label": "familial cardiomyopathy"
    }
  ]
}