{
  "id": 14992,
  "label": "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013982",
  "properties": {
    "xrefs": [
      "DOID:0111653",
      "GARD:0018592",
      "MEDGEN:762105",
      "OMIM:614940",
      "UMLS:C3541517"
    ],
    "synonyms": [
      "ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant",
      "ECTD11A",
      "ectodermal dysplasia, hypohidrotic, autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16602,
      "label": "autosomal dominant hypohidrotic ectodermal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        17032
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002048",
          "MEDGEN:539190",
          "Orphanet:1810",
          "UMLS:C0265331",
          "icd11.foundation:222258115"
        ],
        "synonyms": [
          "AD-HED",
          "autosomal dominant anhidrotic ectodermal dysplasia",
          "hypohidrotic ectodermal dysplasia, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Autosomal dominant form of hypohidrotic ectodermal dysplasia."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015884"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16602,
      "label": "autosomal dominant hypohidrotic ectodermal dysplasia"
    }
  ]
}