{
  "id": 29281,
  "label": "IMPDH1-related retinopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:1040051",
  "properties": {
    "xrefs": [
      "GARD:0027253"
    ],
    "synonyms": [
      "IMPDH1-related retinopathy"
    ],
    "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": "Any retinopathy caused by a variant in the IMPDH1 gene."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19000,
      "label": "inherited retinal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6377,
        21402,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8500",
          "DOID:8501",
          "GARD:0018916",
          "HP:0000556",
          "ICD10CM:H35.5",
          "ICD9:362.7",
          "ICD9:362.70",
          "ICD9:362.72",
          "ICD9:362.75",
          "MEDGEN:208903",
          "MESH:D058499",
          "MedDRA:10038857",
          "NCIT:C35194",
          "NCIT:C35625",
          "Orphanet:71862",
          "SCTID:314407005",
          "SCTID:41799005",
          "UMLS:C0854723"
        ],
        "synonyms": [
          "fundus dystrophy",
          "familial retinal dystrophy",
          "genetic retinal dystrophy",
          "hereditary retinal degeneration",
          "hereditary retinal dystrophy",
          "inherited retinal dystrophy",
          "retinal dystrophy"
        ],
        "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": "An instance of retinal degeneration that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 315,
      "reference_id": "MONDO:0019118"
    }
  ],
  "children": [
    {
      "id": 9678,
      "label": "retinitis pigmentosa 10",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19070,
        29281
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110388",
          "GARD:0015110",
          "MEDGEN:357247",
          "MESH:C566715",
          "OMIM:180105",
          "UMLS:C1867299"
        ],
        "synonyms": [
          "IMPDH1 retinitis pigmentosa",
          "RP10",
          "retinitis pigmentosa 10",
          "retinitis pigmentosa caused by mutation in IMPDH1",
          "retinitis pigmentosa type 10"
        ],
        "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": "Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008379"
    },
    {
      "id": 14485,
      "label": "Leber congenital amaurosis 11",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18914,
        29281
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110216",
          "GARD:0010488",
          "HGNC:6052",
          "MEDGEN:326698",
          "MESH:C564140",
          "OMIM:613837",
          "UMLS:C1840284"
        ],
        "synonyms": [
          "IMPDH1 Leber congenital amaurosis",
          "LCA11",
          "Leber congenital amaurosis 11",
          "Leber congenital amaurosis caused by mutation in IMPDH1",
          "Leber congenital amaurosis type 11",
          "amaurosis congenita of Leber, type 11"
        ],
        "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": "Any Leber congenital amaurosis in which the cause of the disease is a mutation in the IMPDH1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013454"
    }
  ],
  "roots": [
    {
      "id": 19000,
      "label": "inherited retinal dystrophy"
    }
  ]
}