{
  "id": 15423,
  "label": "glucocorticoid resistance",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014421",
  "properties": {
    "xrefs": [
      "GARD:0002499",
      "MEDGEN:333960",
      "MESH:C564221",
      "NANDO:2200358",
      "OMIM:615962",
      "Orphanet:786",
      "UMLS:C1841972",
      "icd11.foundation:125216923"
    ],
    "synonyms": [
      "GCCR",
      "Gccr deficiency",
      "Gcr deficiency",
      "Grl deficiency",
      "cortisol resistance from glucocorticoid receptor defect",
      "glucocorticoid receptor deficiency",
      "glucocorticoid resistance, generalised",
      "glucocorticoid resistance, generalized"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3146",
          "GARD:0021314",
          "ICD9:272.8",
          "ICD9:272.9",
          "MEDGEN:57587",
          "MedDRA:10061227",
          "NCIT:C97092",
          "Orphanet:309005",
          "SCTID:267431006",
          "SCTID:402788005",
          "UMLS:C0154251"
        ],
        "synonyms": [
          "disorder of lipid metabolism",
          "dyslipidaemia",
          "dyslipidemia",
          "lipid metabolism disorder",
          "fatty acid metabolism disorder"
        ],
        "definition": "An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production."
      },
      "child_count": 29,
      "reference_id": "MONDO:0002525"
    },
    {
      "id": 16604,
      "label": "adrenogenital syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7151,
        23508
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020226",
          "ICD9:255.2",
          "MEDGEN:86215",
          "MESH:D047808",
          "MedDRA:10061630",
          "Orphanet:181412",
          "SCTID:267395000",
          "UMLS:C0302280",
          "icd11.foundation:131153029"
        ],
        "synonyms": [
          "adrenogenital disorder",
          "adrenogenital syndrome",
          "androgenital syndrome",
          "congenital adrenal hyperplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Abnormal sex differentiation or congenital disorders of sex development caused by abnormal levels of steroid hormones expressed by the gonads or the adrenal glands, such as in congenital adrenal hyperplasia and adrenal cortex neoplasms. Due to abnormal steroid biosynthesis, clinical features include virilism in females; feminization in males; or precocious sexual development in children."
      },
      "child_count": 8,
      "reference_id": "MONDO:0015898"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder"
    },
    {
      "id": 16604,
      "label": "adrenogenital syndrome"
    }
  ]
}