{
  "id": 3606,
  "label": "myopia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001384",
  "properties": {
    "xrefs": [
      "DOID:11830",
      "HP:0000545",
      "ICD10CM:H52.1",
      "ICD9:367.1",
      "MEDGEN:44558",
      "MESH:D009216",
      "OMIMPS:160700",
      "SCTID:57190000",
      "UMLS:C0027092",
      "icd11.foundation:1666440799"
    ],
    "synonyms": [
      "myopia",
      "myopia (disease)",
      "near-sightedness"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "The condition in which the individual does not see far distances clearly."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 30,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 6646,
      "label": "refractive error",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9835",
          "MEDGEN:20508",
          "MESH:D012030",
          "SCTID:39021009",
          "UMLS:C0034951"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A defect in the focusing of light on the retina as in astigmatism, myopia, or hyperopia."
      },
      "child_count": 7,
      "reference_id": "MONDO:0004892"
    },
    {
      "id": 24305,
      "label": "ocular growth disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An eye disorder characterized by an aberrant development of the eye resulting in significant shortening or elongation, and therefore affecting the final ocular dimensions."
      },
      "child_count": 7,
      "reference_id": "MONDO:0100581"
    }
  ],
  "children": [
    {
      "id": 3605,
      "label": "degenerative myopia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606,
        6639
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11829",
          "GARD:0022930",
          "ICD10CM:H44.2",
          "ICD9:360.21",
          "MEDGEN:57597",
          "MESH:D047728",
          "SCTID:32022003",
          "UMLS:C0154778"
        ],
        "synonyms": [
          "progressive high (degenerative) myopia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Excessive axial myopia associated with complications (especially posterior staphyloma and choroidal neovascularization) that can lead to blindness."
      },
      "child_count": 0,
      "reference_id": "MONDO:0001383"
    },
    {
      "id": 9376,
      "label": "myopia 2, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:331770",
          "MESH:C563541",
          "OMIM:160700",
          "UMLS:C1834531"
        ],
        "synonyms": [
          "MYP2",
          "myopia 2, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008053"
    },
    {
      "id": 10926,
      "label": "myopia 18, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:411856",
          "MESH:C567606",
          "OMIM:255500",
          "UMLS:C2749509"
        ],
        "synonyms": [
          "MYP18",
          "myopia 18, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009713"
    },
    {
      "id": 11540,
      "label": "myopia 13, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:335097",
          "MESH:C564473",
          "OMIM:300613",
          "UMLS:C1845096"
        ],
        "synonyms": [
          "MYP13",
          "myopia 13",
          "myopia 13, X-linked"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010377"
    },
    {
      "id": 11829,
      "label": "myopia 1, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:326540",
          "MESH:C564091",
          "OMIM:310460",
          "UMLS:C1839612"
        ],
        "synonyms": [
          "MYP1",
          "myopia 1, X-linked",
          "myopia-1, X-linked recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010685"
    },
    {
      "id": 12416,
      "label": "myopia 3, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:400454",
          "MESH:C566397",
          "OMIM:603221",
          "UMLS:C1864111"
        ],
        "synonyms": [
          "MYP3",
          "myopia 3, autosomal dominant",
          "myopia-3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011300"
    },
    {
      "id": 13090,
      "label": "myopia 17, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:854818",
          "OMIM:608367",
          "UMLS:C3888211"
        ],
        "synonyms": [
          "MYP17",
          "myopia 17, autosomal dominant",
          "myopia 4",
          "myopia 4, formerly"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012021"
    },
    {
      "id": 13113,
      "label": "myopia 5, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:324913",
          "MESH:C563922",
          "OMIM:608474",
          "UMLS:C1837972"
        ],
        "synonyms": [
          "MYP5",
          "myopia 5, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012045"
    },
    {
      "id": 13217,
      "label": "myopia 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009937",
          "MEDGEN:324696",
          "MESH:C536105",
          "OMIM:608908",
          "UMLS:C1837148"
        ],
        "synonyms": [
          "SCO2 myopia (disease)",
          "myopia (disease) caused by mutation in SCO2",
          "myopia 6",
          "myopia type 6",
          "MYP6",
          "myopia, susceptibility to"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any myopia in which the cause of the disease is a mutation in the SCO2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012154"
    },
    {
      "id": 13288,
      "label": "myopia 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:373105",
          "MESH:C563761",
          "OMIM:609256",
          "UMLS:C1836506"
        ],
        "synonyms": [
          "MYP7",
          "myopia 7"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012227"
    },
    {
      "id": 13289,
      "label": "myopia 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:332223",
          "MESH:C563760",
          "OMIM:609257",
          "UMLS:C1836505"
        ],
        "synonyms": [
          "MYP8",
          "myopia 8"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012228"
    },
    {
      "id": 13290,
      "label": "myopia 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:332222",
          "MESH:C563759",
          "OMIM:609258",
          "UMLS:C1836504"
        ],
        "synonyms": [
          "MYP9",
          "myopia 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012229"
    },
    {
      "id": 13291,
      "label": "myopia 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:373104",
          "MESH:C563758",
          "OMIM:609259",
          "UMLS:C1836503"
        ],
        "synonyms": [
          "MYP10",
          "myopia 10"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012230"
    },
    {
      "id": 13439,
      "label": "myopia 11, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:355874",
          "MESH:C566490",
          "OMIM:609994",
          "UMLS:C1864941"
        ],
        "synonyms": [
          "MYP11",
          "myopia 11",
          "myopia 11, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012388"
    },
    {
      "id": 13440,
      "label": "myopia 12, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:355332",
          "MESH:C566489",
          "OMIM:609995",
          "UMLS:C1864940"
        ],
        "synonyms": [
          "MYP12",
          "myopia 12",
          "myopia 12, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012389"
    },
    {
      "id": 13518,
      "label": "myopia 14",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:343990",
          "MESH:C565202",
          "OMIM:610320",
          "UMLS:C1853196"
        ],
        "synonyms": [
          "MYP14",
          "myopia 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012469"
    },
    {
      "id": 13972,
      "label": "myopia 16, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:390819",
          "MESH:C567259",
          "OMIM:612554",
          "UMLS:C2675523"
        ],
        "synonyms": [
          "MYP16",
          "myopia 16",
          "myopia 16, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012932"
    },
    {
      "id": 14035,
      "label": "myopia 15, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:393323",
          "MESH:C567193",
          "OMIM:612717",
          "UMLS:C2675180"
        ],
        "synonyms": [
          "MYP15",
          "myopia 15, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012995"
    },
    {
      "id": 14536,
      "label": "schizophrenia 16",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606,
        6817,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070092",
          "MEDGEN:462758",
          "OMIM:613959",
          "UMLS:C3151408"
        ],
        "synonyms": [
          "SCZD16",
          "schizophrenia 16",
          "schizophrenia type 16",
          "chromosome 7Q36.3 Duplication syndrome, 362-Kb",
          "schizophrenia susceptibility locus, chromosome 7Q36.3-related"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A schizophrenia that has material basis in a mutation on chromosome 7q36.3."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013506"
    },
    {
      "id": 14538,
      "label": "myopia 19, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:462760",
          "OMIM:613969",
          "UMLS:C3151410"
        ],
        "synonyms": [
          "MYP19",
          "myopia 19, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013508"
    },
    {
      "id": 14629,
      "label": "myopia 20, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:481626",
          "OMIM:614166",
          "UMLS:C3279996"
        ],
        "synonyms": [
          "MYP20",
          "myopia 20, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013603"
    },
    {
      "id": 14630,
      "label": "myopia 21, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:481627",
          "OMIM:614167",
          "UMLS:C3279997"
        ],
        "synonyms": [
          "ZNF644 myopia (disease)",
          "myopia (disease) caused by mutation in ZNF644",
          "myopia 21, autosomal dominant",
          "MYP21"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013604"
    },
    {
      "id": 14693,
      "label": "myopia, high, with cataract and vitreoretinal degeneration",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018197",
          "MEDGEN:481976",
          "OMIM:614292",
          "UMLS:C3280346"
        ],
        "synonyms": [
          "myopia, high, with cataract and vitreoretinal degeneration",
          "MCVD"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0013670"
    },
    {
      "id": 15184,
      "label": "myopia 22, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:815794",
          "OMIM:615420",
          "UMLS:C3809464"
        ],
        "synonyms": [
          "myopia 22, autosomal dominant",
          "MYP22"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014177"
    },
    {
      "id": 15190,
      "label": "myopia 23, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018198",
          "MEDGEN:815812",
          "OMIM:615431",
          "UMLS:C3809482"
        ],
        "synonyms": [
          "myopia 23, autosomal recessive",
          "MYP23"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014183"
    },
    {
      "id": 15413,
      "label": "myopia 24, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:863199",
          "OMIM:615946",
          "UMLS:C4014762"
        ],
        "synonyms": [
          "myopia 24, autosomal dominant",
          "MYP24"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014411"
    },
    {
      "id": 15959,
      "label": "myopia 25, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:934622",
          "OMIM:617238",
          "UMLS:C4310655"
        ],
        "synonyms": [
          "MYP25",
          "P4HA2 myopia (disease)",
          "myopia (disease) caused by mutation in P4HA2",
          "myopia 25, autosomal dominant",
          "myopia 25, autosomal dominant; MYP25"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Any myopia (disease) in which the cause of the disease is a mutation in the P4HA2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014982"
    },
    {
      "id": 22006,
      "label": "myopia 28, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1806812",
          "OMIM:619781",
          "UMLS:C5676935"
        ],
        "synonyms": [
          "MYP28",
          "myopia 28, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0030697"
    },
    {
      "id": 22592,
      "label": "myopia 27",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1719756",
          "OMIM:618827",
          "UMLS:C5394215"
        ],
        "synonyms": [
          "MYOPIA 27",
          "MYP27"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032941"
    },
    {
      "id": 23553,
      "label": "myopia 26, X-linked, female-limited",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3606
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1618364",
          "OMIM:301010",
          "UMLS:C4538795"
        ],
        "synonyms": [
          "myopia 26, X-linked, female-limited",
          "MYP26"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0049221"
    }
  ],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 6646,
      "label": "refractive error"
    },
    {
      "id": 24305,
      "label": "ocular growth disorder"
    }
  ]
}