{
  "id": 9004,
  "label": "Sorsby fundus dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007640",
  "properties": {
    "xrefs": [
      "DOID:0090114",
      "GARD:0016480",
      "MEDGEN:338164",
      "MESH:C564992",
      "OMIM:136900",
      "Orphanet:59181",
      "SCTID:193410003",
      "UMLS:C1850938",
      "icd11.foundation:796458172"
    ],
    "synonyms": [
      "SFD",
      "Sorsby fundus dystrophy",
      "Sorsby pseudoinflammatory fundus dystrophy",
      "Sorsby's pseudoinflammatory macular dystrophy",
      "fundus dystrophy, pseudoinflammatory, of Sorsby",
      "macular dystrophy, hemorrhagic"
    ],
    "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 rare progressive autosomal dominant macular dystrophy, presenting between the third and sixth decades of life, characterized by retinal atrophy and retinal detachment and leading to loss of central vision, then peripheral vision, and eventually blindness."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "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": 11121,
      "label": "fundus dystrophy, pseudoinflammatory, recessive form",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9004
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009633",
          "MEDGEN:337888",
          "MESH:C535828",
          "OMIM:264420",
          "UMLS:C1849694"
        ],
        "synonyms": [
          "fundus dystrophy, pseudoinflammatory, recessive form",
          "PFD Lavia type",
          "Pfd, Finnish type",
          "Pfd, Lavia type",
          "fundus dystrophy, pseudoinflammatory recessive form",
          "pseudoinflammatory fundus 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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0009918"
    }
  ],
  "roots": [
    {
      "id": 19000,
      "label": "inherited retinal dystrophy"
    }
  ]
}