{
  "id": 12519,
  "label": "Peters anomaly",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011414",
  "properties": {
    "xrefs": [
      "DOID:0060673",
      "DOID:0080610",
      "GARD:0007377",
      "HP:0000659",
      "ICD9:743.44",
      "MEDGEN:91031",
      "MESH:C537884",
      "MedDRA:10059202",
      "OMIM:604229",
      "Orphanet:708",
      "SCTID:204153003",
      "UMLS:C0344559",
      "icd11.foundation:1902926622"
    ],
    "synonyms": [
      "Peters anomaly",
      "Peters anomaly (disease)",
      "Peters congenital glaucoma",
      "anterior segment dysgenesis 5, multiple subtypes",
      "ASGD5",
      "anterior segment dysgenesis 5"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Peters anomaly (PA) is a congenital corneal opacity disorder characterized by a central corneal leukoma that obstructs the pupil leading to visual loss as well as absence of the posterior corneal stroma and Descemet membrane."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 3211,
      "label": "corneal disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10124",
          "EFO:0009464",
          "ICD9:371.30",
          "ICD9:371.89",
          "ICD9:371.9",
          "MEDGEN:3617",
          "MESH:D003316",
          "NCIT:C26731",
          "SCTID:15250008",
          "UMLS:C0010034",
          "icd11.foundation:980864631"
        ],
        "synonyms": [
          "cornea disease",
          "cornea disease or disorder",
          "corneal disease",
          "corneal disorder",
          "disease of cornea",
          "disease or disorder of cornea",
          "disorder of cornea"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the cornea. Representative examples include keratitis, bullous keratopathy, and squamous cell carcinoma."
      },
      "child_count": 24,
      "reference_id": "MONDO:0000942"
    },
    {
      "id": 19321,
      "label": "anterior segment dysgenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        7019,
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060648",
          "GARD:0010025",
          "ICD9:743.49",
          "MEDGEN:350766",
          "NANDO:1201000",
          "OMIMPS:107250",
          "Orphanet:88632",
          "SCTID:65075004",
          "UMLS:C1862839",
          "icd11.foundation:1182282997",
          "icd11.foundation:943599144"
        ],
        "synonyms": [
          "ASGD",
          "ASMD",
          "ASOD",
          "anterior segment mesenchymal dysgenesis",
          "anterior segment ocular dysgenesis",
          "familial ocular anterior segment mesenchymal dysgenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A spectrum of developmental anomalies that affect the development of the anterior segment of the eyeball resulting from abnormalities of neural crest migration and differentiation during embryologic development (Axenfeld-Rieger syndrome, Peters anomaly, posterior keratoconus, and iridoschisis)."
      },
      "child_count": 24,
      "reference_id": "MONDO:0019503"
    }
  ],
  "children": [
    {
      "id": 16061,
      "label": "Peters anomaly-cataract syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        12519
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025060",
          "MEDGEN:419463",
          "MESH:C537885",
          "Orphanet:101033",
          "UMLS:C2931652"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015095"
    },
    {
      "id": 19815,
      "label": "von Hippel anomaly",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        12519
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "Orphanet:98941",
          "icd11.foundation:1620371681"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020353"
    }
  ],
  "roots": [
    {
      "id": 3211,
      "label": "corneal disorder"
    },
    {
      "id": 19321,
      "label": "anterior segment dysgenesis"
    }
  ]
}