{
  "id": 7020,
  "label": "hyperthyroxinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0005333",
  "properties": {
    "xrefs": [
      "DOID:2855",
      "EFO:0004127",
      "HGNC:399",
      "MEDGEN:6973",
      "MESH:D006981",
      "UMLS:C0020551"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Abnormally elevated thyroxine level in the blood."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 5187,
      "label": "thyroid gland disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:50",
          "EFO:1000627",
          "ICD10CM:E00-E07",
          "ICD9:240-246",
          "ICD9:246.8",
          "ICD9:246.9",
          "MEDGEN:1378579",
          "MESH:D013959",
          "NCIT:C26893",
          "SCTID:14304000",
          "UMLS:C4317107",
          "Wikipedia:Thyroid_disease"
        ],
        "synonyms": [
          "disease of thyroid gland",
          "disease or disorder of thyroid gland",
          "disorder of thyroid gland",
          "thyroid disease",
          "thyroid gland disease",
          "thyroid gland disease or disorder",
          "thyroid gland diseases",
          "thyroid gland disorder",
          "thyroid gland disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the thyroid gland."
      },
      "child_count": 12,
      "reference_id": "MONDO:0003240"
    }
  ],
  "children": [
    {
      "id": 9131,
      "label": "hyperthyroxinemia, dystransthyretinemic",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        7020
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080219",
          "MEDGEN:442573",
          "MESH:C567719",
          "OMIM:145680",
          "UMLS:C2750824"
        ],
        "synonyms": [
          "hyperthyroxinemia, dystransthyretinemic",
          "DTTRH",
          "dystransthyretinemic ethyroidal hyperthyroxinemia",
          "euthryroidal hyperthyroxinemia 2",
          "hyperthyroxinemia, Dysprealbuminemic"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007785"
    },
    {
      "id": 15448,
      "label": "hyperthyroxinemia, familial dysalbuminemic",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        6233,
        7020
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:90974",
          "MESH:D050010",
          "NCIT:C131813",
          "OMIM:615999",
          "Orphanet:276271",
          "SCTID:237547004",
          "UMLS:C0342185"
        ],
        "synonyms": [
          "bisalbuminemia",
          "dysalbuminemic hyperthyroxinemia",
          "dysalbuminemic hypertriiodothyroninemia",
          "familial Dysalbuminemic hyperthyroidism",
          "familial Dysalbuminemic hyperthyroxinemia",
          "hyperthyroxinemia, familial Dysalbuminemic",
          "hyperthyroxinemia, familial dysalbuminemic",
          "FDAH",
          "FDH",
          "euthyroid hyperthyroxinemia 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum thyroxine; (T4) in euthyroid patients with abnormal serum albumin that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and tsh are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the alb gene on chromosome 4."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014448"
    },
    {
      "id": 22932,
      "label": "euthyroid dysprealbuminemic hyperthyroxinemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7020
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022401",
          "MEDGEN:1842463",
          "Orphanet:597939",
          "UMLS:C5680265"
        ],
        "synonyms": [
          "Euthyroid dystransthyretinemic hyperthyroxinemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0036045"
    }
  ],
  "roots": [
    {
      "id": 5187,
      "label": "thyroid gland disorder"
    }
  ]
}