{
  "id": 20388,
  "label": "X-linked cone-rod dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021155",
  "properties": {
    "xrefs": [
      "GARD:0025295"
    ],
    "synonyms": [
      "cone-rod dystrophy, X-linked"
    ],
    "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": "X-linked form of cone-rod dystrophy."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 16636,
      "label": "cone-rod dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050572",
          "GARD:0010790",
          "MEDGEN:896366",
          "MESH:D000071700",
          "NANDO:1200937",
          "OMIMPS:120970",
          "Orphanet:1872",
          "UMLS:C4085590"
        ],
        "synonyms": [
          "CRD",
          "cone rod 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": "Inherited retinal dystrophies that belong to the group of pigmentary retinopathies."
      },
      "child_count": 28,
      "reference_id": "MONDO:0015993"
    }
  ],
  "children": [
    {
      "id": 11421,
      "label": "X-linked cone-rod dystrophy 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20388
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111006",
          "GARD:0001462",
          "MEDGEN:341161",
          "MESH:C564717",
          "OMIM:300085",
          "UMLS:C1848139"
        ],
        "synonyms": [
          "COD2",
          "CORDX2",
          "X-linked cone-rod dystrophy type 2",
          "cone dystrophy 2, X-linked",
          "cone dystrophy X-linked 2",
          "cone dystrophy, progressive X-linked, 2",
          "cone-rod dystrophy X-linked 2",
          "cone-rod dystrophy, X-linked, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010245"
    },
    {
      "id": 11504,
      "label": "X-linked cone-rod dystrophy 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20388,
        24638
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111007",
          "GARD:0010654",
          "MEDGEN:336932",
          "MESH:C564507",
          "OMIM:300476",
          "UMLS:C1845407"
        ],
        "synonyms": [
          "CORDX3",
          "X-linked cone-rod dystrophy type 3",
          "cone-rod dystrophy, X-linked, 3, X-linked recessive",
          "cone-rod dystrophy, X-linked, type 3",
          "cone-rod dystrophy X-linked 3",
          "cone-rod dystrophy, X-linked, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010335"
    },
    {
      "id": 11717,
      "label": "blue cone monochromacy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18788,
        20040,
        20388
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050679",
          "GARD:0000917",
          "MEDGEN:87386",
          "MESH:C536238",
          "OMIM:303700",
          "Orphanet:16",
          "SCTID:24704003",
          "UMLS:C0339537"
        ],
        "synonyms": [
          "S cone monochromacy",
          "S cone monochromatism",
          "X-linked incomplete achromatopsia",
          "atypical X-linked achromatopsia",
          "blue cone monochromacy",
          "blue cone monochromacy, X-linked recessive",
          "blue cone monochromatism",
          "color blindness, blue monocone monochromatic type",
          "colour blindness, blue monocone monochromatic type",
          "BCM",
          "CBBM",
          "X-chromosome-linked achromatopsia",
          "X-linked achromatopsia incomplete",
          "achromatopsia incomplete X-linked",
          "color blindness blue mono cone monochromatic type",
          "colorblindness, blue-Mono-cone-monochromatic type",
          "colour blindness blue mono cone monochromatic type",
          "cone dystrophy 5, X-linked",
          "incomplete achromatopsia X-linked"
        ],
        "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": "Blue cone monochromatism (BCM) is a recessive X-linked disease characterized by severely impaired color discrimination, low visual acuity, nystagmus, and photophobia, due to dysfunction of the red (L) and green (M) cone photoreceptors. BCM is as an incomplete form of achromatopsia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010563"
    },
    {
      "id": 11720,
      "label": "X-linked cone-rod dystrophy 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        20388,
        24164
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111008",
          "GARD:0010652",
          "MEDGEN:336777",
          "MESH:C564438",
          "OMIM:304020",
          "UMLS:C1844776"
        ],
        "synonyms": [
          "CORDX1",
          "X-linked cone-rod dystrophy type 1",
          "cone-rod dystrophy, X-linked, 1, X-linked recessive",
          "cone-rod dystrophy, X-linked, type 1",
          "cone dystrophy 1, X-linked",
          "cone dystrophy X-linked 1",
          "cone-rod dystrophy X-linked 1",
          "cone-rod dystrophy, X-linked, 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010566"
    }
  ],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 16636,
      "label": "cone-rod dystrophy"
    }
  ]
}