{
  "id": 8771,
  "label": "posterior polymorphous corneal dystrophy 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007378",
  "properties": {
    "xrefs": [
      "DOID:0110855",
      "GARD:0018212",
      "ICD9:371.58",
      "MEDGEN:343836",
      "OMIM:122000",
      "SCTID:29504002",
      "UMLS:C1852555"
    ],
    "synonyms": [
      "Maumenee corneal dystrophy",
      "PPCD1",
      "Ppcd1",
      "corneal dystrophy, posterior polymorphous, type 1",
      "posterior polymorphous corneal dystrophy type 1",
      "corneal dystrophy, POSTERIOR polymorphous, 1",
      "corneal dystrophy, hereditary polymorphous posterior",
      "corneal endothelial dystrophy 1, autosomal dominant, formerly",
      "posterior polymorphous corneal dystrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A posterior polymorphous corneal dystrophy that has material basis in autosomal dominant inheritance of mutation in the OVOL2 gene on chromosome 20p11.23."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19825,
      "label": "posterior polymorphous corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3132,
        5714,
        19764
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060457",
          "GARD:0016882",
          "MEDGEN:87382",
          "OMIMPS:122000",
          "Orphanet:98973",
          "UMLS:C0339284",
          "icd11.foundation:935421185"
        ],
        "synonyms": [
          "PPCD",
          "Schlichting dystrophy",
          "corneal dystrophy, posterior polymorphous",
          "posterior polymorphous dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Posterior polymorphous corneal dystrophy (PPCD) is a rare mild subtype of posterior corneal dystrophy characterized by small aggregates of apparent vesicles bordered by a gray haze at the level of Descemet membrane, generally with no effect on vision."
      },
      "child_count": 12,
      "reference_id": "MONDO:0020364"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19825,
      "label": "posterior polymorphous corneal dystrophy"
    }
  ]
}