{
  "id": 20123,
  "label": "thyroid dyshormonogenesis 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020716",
  "properties": {
    "xrefs": [
      "DOID:0112185",
      "GARD:0018188",
      "MEDGEN:336422",
      "OMIM:274400",
      "UMLS:C1848805"
    ],
    "synonyms": [
      "TDH1",
      "familial thyroid dyshormonogenesis 1",
      "hypothyroidism, congenital, due to dyshormonogenesis, 1",
      "iodine accumulation, transport, or trapping defect",
      "thyroid dyshormonogenesis type 1",
      "thyroid hormonogenesis, genetic defect in, 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11315,
      "label": "familial thyroid dyshormonogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18613,
        23532
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112183",
          "GARD:0016843",
          "MEDGEN:903446",
          "MESH:C564766",
          "NCIT:C121751",
          "OMIMPS:274400",
          "Orphanet:95716",
          "SCTID:718183003",
          "UMLS:C4273748"
        ],
        "synonyms": [
          "dyshormonogenesis",
          "nongoitrous hyperthyrotropinemia",
          "thyroid dyshormonogenesis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis."
      },
      "child_count": 12,
      "reference_id": "MONDO:0010132"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11315,
      "label": "familial thyroid dyshormonogenesis"
    }
  ]
}