{
  "id": 10024,
  "label": "corticosterone methyloxidase type 1 deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008751",
  "properties": {
    "xrefs": [
      "DOID:0080626",
      "GARD:0005660",
      "MEDGEN:82784",
      "OMIM:203400",
      "SCTID:47757001",
      "UMLS:C0268293"
    ],
    "synonyms": [
      "corticosterone 18-monooxygenase deficiency",
      "corticosterone methyloxidase type 1 deficiency",
      "hypoaldosteronism, congenital, due to cmo i deficiency",
      "18 Hydroxylase deficiency",
      "18 alpha hydroxylase deficiency",
      "18-Hydroxylase deficiency",
      "18-hydroxycorticosterone dehydrogenase deficiency",
      "18-hydroxylase deficiency",
      "CAH - 18-hydroxylase deficiency",
      "CMO 1 deficiency",
      "CMO I deficiency",
      "CMO II deficiency",
      "aldosterone deficiency 1",
      "aldosterone deficiency due to 18-hydroxylase defect",
      "aldosterone deficiency due to 18-hydroxysteroid dehydrogenase deficiency",
      "aldosterone deficiency due to defect in 18 hydroxylase",
      "aldosterone deficiency due to defect in steroid 18-Hydroxylase",
      "corticosterone methyl oxidase type I deficiency",
      "corticosterone methyl oxidase type II deficiency",
      "corticosterone methyloxidase type I deficiency",
      "hyperreninemic hypoaldosteronism, familial, 1",
      "steroid 18-hydroxylase deficiency"
    ],
    "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": 18558,
      "label": "familial hypoaldosteronism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16605
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016532",
          "MEDGEN:899592",
          "Orphanet:427",
          "SCTID:715343000",
          "UMLS:C4275180",
          "icd11.foundation:712299654"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Aldosterone synthase deficiency is a rare inherited defect of the final step of aldosterone biosynthesis (conversion of deoxycorticosterone to aldosterone)."
      },
      "child_count": 5,
      "reference_id": "MONDO:0018541"
    },
    {
      "id": 23508,
      "label": "steroid metabolism disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6795
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:541265",
          "SCTID:28710006",
          "UMLS:C0268283"
        ],
        "synonyms": [
          "disorder of steroid metabolic process",
          "disorder of steroid metabolism",
          "steroid metabolic process disease",
          "steroid metabolism disease"
        ],
        "definition": "A disease that has its basis in the disruption of steroid metabolic process."
      },
      "child_count": 4,
      "reference_id": "MONDO:0045012"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder"
    },
    {
      "id": 18558,
      "label": "familial hypoaldosteronism"
    },
    {
      "id": 23508,
      "label": "steroid metabolism disease"
    }
  ]
}