{
  "id": 12907,
  "label": "glucocorticoid deficiency 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011826",
  "properties": {
    "xrefs": [
      "DOID:0061242",
      "GARD:0015412",
      "MEDGEN:891117",
      "MESH:C564577",
      "NANDO:1200409",
      "NCIT:C123728",
      "OMIM:607398",
      "UMLS:C4049714"
    ],
    "synonyms": [
      "MRAP familial glucocorticoid deficiency",
      "familial glucocorticoid deficiency caused by mutation in MRAP",
      "glucocorticoid deficiency 2",
      "glucocorticoid deficiency type 2",
      "GCCD2",
      "familial glucocorticoid deficiency 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MRAP gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10006,
      "label": "familial glucocorticoid deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16074
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080620",
          "GARD:0002498",
          "MEDGEN:885955",
          "MESH:C565974",
          "NCIT:C120446",
          "OMIMPS:202200",
          "Orphanet:361",
          "SCTID:765326001",
          "UMLS:C4054695",
          "icd11.foundation:861297039"
        ],
        "synonyms": [
          "glucocorticoid deficiency",
          "GCCD"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Familial glucocorticoid deficiency (FGD) is a group of primary adrenal insufficiencies characterized clinically by neonatal hyperpigmentation, hypoglycemia, failure to thrive, and recurrent infections, and biochemically by glucocorticoid deficiency without mineralocorticoid deficiency."
      },
      "child_count": 12,
      "reference_id": "MONDO:0008733"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10006,
      "label": "familial glucocorticoid deficiency"
    }
  ]
}