{
  "id": 20093,
  "label": "Ehlers-Danlos syndrome, periodontal type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020684",
  "properties": {
    "xrefs": [
      "DOID:0080986",
      "GARD:0025210",
      "MEDGEN:1642148",
      "OMIM:130080",
      "UMLS:C4551499"
    ],
    "synonyms": [
      "EDS 8",
      "EDSPD1",
      "Ehlers-Danlos syndrome, periodontal type, 1",
      "Ehlers-Danlos syndrome, periodontitis type",
      "Ehlers-Danlos syndrome, periodontosis type",
      "Ehlers-Danlos syndrome, type 8"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8909,
      "label": "Ehlers-Danlos syndrome, periodontitis type",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19720
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012474",
          "MEDGEN:82791",
          "MESH:C562626",
          "Orphanet:75392",
          "SCTID:50869007",
          "UMLS:C0268347",
          "icd11.foundation:893527307"
        ],
        "synonyms": [
          "EDS VIII",
          "Ehlers-Danlos syndrome type 8",
          "Ehlers-Danlos syndrome, periodontitis type",
          "EDS 8",
          "EDS VIII (formerly)",
          "EDS8",
          "EDS8 (formerly)",
          "Ehlers-Danlos syndrome type 8 (formerly)",
          "Ehlers-Danlos syndrome, periodontosis type",
          "Ehlers-Danlos syndrome, type 8",
          "Ehlers-Danlos syndrome, type VIII",
          "Ehlers-Danlos syndrome, type VIII (formerly)",
          "pEDS",
          "periodontal EDS",
          "periodontal Ehlers-Danlos syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility."
      },
      "child_count": 2,
      "reference_id": "MONDO:0007527"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8909,
      "label": "Ehlers-Danlos syndrome, periodontitis type"
    }
  ]
}