{
  "id": 10391,
  "label": "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009147",
  "properties": {
    "xrefs": [
      "DOID:0111665",
      "GARD:0015163",
      "MEDGEN:854356",
      "OMIM:224900",
      "UMLS:C3887494"
    ],
    "synonyms": [
      "ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive",
      "ECTD10B",
      "ectodermal dysplasia, anhidrotic",
      "ectodermal dysplasia, hypohidrotic"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17103,
      "label": "autosomal recessive hypohidrotic ectodermal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        17032
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0002057",
          "MEDGEN:96067",
          "MESH:D053360",
          "NCIT:C84580",
          "Orphanet:248",
          "SCTID:27025001",
          "UMLS:C0406702",
          "icd11.foundation:7083042"
        ],
        "synonyms": [
          "AR-HED",
          "autosomal recessive anhidrotic ectodermal dysplasia",
          "hypohidrotic ectodermal dysplasia, autosomal recessive",
          "anhidrotic ectodermal dysplasia, autosomal recessive",
          "hypohidrotic ectodermal dysplasia autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A rare autosomal recessive disorder characterized by developmental abnormalities of the skin, sweat glands, hair and nails. Patients have a reduced ability to sweat. Other signs and symptoms include hypotrichosis and teeth malformations."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016619"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17103,
      "label": "autosomal recessive hypohidrotic ectodermal dysplasia"
    }
  ]
}