{
  "id": 20118,
  "label": "selective peripheral resistance to thyroid hormone",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020711",
  "properties": {
    "xrefs": [
      "GARD:0025218"
    ],
    "synonyms": [
      "PerRTH"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A thyroid hormone resistance syndrome characterized by resistance in peripheral tissues but not in the pituitary."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3557,
      "label": "thyroid hormone resistance syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        23532
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11633",
          "GARD:0022922",
          "ICD9:259.8",
          "MEDGEN:424854",
          "MESH:D018382",
          "NANDO:1200395",
          "NANDO:2100121",
          "NANDO:2200341",
          "SCTID:111567006",
          "UMLS:C2940786"
        ],
        "synonyms": [
          "generalised thyroid hormone resistance",
          "RTH",
          "TSH resistance",
          "resistance to thyroid stimulating hormone",
          "resistance to thyrotropin"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An inherited autosomal recessive trait, characterized by peripheral resistance to thyroid hormones and the resulting elevation in serum levels of thyroxine and triiodothyronine."
      },
      "child_count": 4,
      "reference_id": "MONDO:0001328"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3557,
      "label": "thyroid hormone resistance syndrome"
    }
  ]
}