{
  "id": 8767,
  "label": "Schnyder corneal dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007374",
  "properties": {
    "xrefs": [
      "DOID:0060456",
      "GARD:0009277",
      "MEDGEN:124391",
      "MESH:C535475",
      "OMIM:121800",
      "Orphanet:98967",
      "SCTID:419395007",
      "UMLS:C0271287"
    ],
    "synonyms": [
      "SCCD",
      "SCD",
      "Schnyder corneal dystrophy",
      "Schnyder crystalline corneal dystrophy",
      "Schnyder crystalline dystrophy sine crystals",
      "corneal dystrophy, Schnyder type",
      "crystalline stromal dystrophy",
      "hereditary crystalline stromal dystrophy of Schnyder",
      "corneal dystrophy, Schnyder",
      "corneal dystrophy, crystalline, of Schnyder"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Schnyder corneal dystrophy (SCD) is a rare form of stromal corneal dystrophy characterized by corneal clouding or crystals within the corneal stroma, and a progressive decrease in visual acuity."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 19763,
      "label": "stromal corneal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18261
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060442",
          "GARD:0019519",
          "ICD9:371.56",
          "MEDGEN:20973",
          "Orphanet:98626",
          "SCTID:231931001",
          "UMLS:C0038457",
          "icd11.foundation:1392780216"
        ],
        "synonyms": [
          "corneal dystrophy (disease) of substantia propria of cornea",
          "corneal stromal dystrophy",
          "substantia propria of cornea corneal dystrophy (disease)",
          "stromal dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "The stromal corneal dystrophies refer to a group of rare genetically determined corneal dystrophies (CDs) characterized by lesions affecting the corneal stroma, and variable effects on vision depending on the type of dystrophy."
      },
      "child_count": 10,
      "reference_id": "MONDO:0020213"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 19763,
      "label": "stromal corneal dystrophy"
    }
  ]
}