{
  "id": 11423,
  "label": "X-linked cerebral adrenoleukodystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010247",
  "properties": {
    "xrefs": [
      "GARD:0009412",
      "MEDGEN:1708324",
      "NANDO:1200166",
      "NANDO:2201246",
      "Orphanet:139396",
      "UMLS:C2026514",
      "icd11.foundation:1105019687"
    ],
    "synonyms": [
      "X-linked cerebral adrenoleukodystrophy",
      "ALD",
      "ALD childhood cerebral form",
      "Addison disease and cerebral sclerosis",
      "Siemerling-Creutzfeldt disease",
      "adrenoleukodystrophy",
      "adrenoleukodystrophy X-linked cerebral form",
      "adrenoleukodystrophy childhood cerebral form",
      "adrenomyeloneuropathy",
      "bronze Schilder disease",
      "childhood cerebral ALD",
      "childhood-onset cerebral X-linked adrenoleukodystrophy",
      "melanodermic leukodystrophy"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A peroxisomal disease characterized by severe inflammatory demyelination in the brain, and often associated with adrenal insufficiency."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18561,
      "label": "adrenoleukodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2902,
        7151,
        16360,
        18952,
        24100
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10588",
          "GARD:0005758",
          "MEDGEN:57667",
          "MESH:D000326",
          "MedDRA:10051260",
          "NANDO:1200165",
          "NANDO:2200576",
          "NCIT:C61252",
          "NORD:736",
          "OMIM:300100",
          "Orphanet:43",
          "UMLS:C0162309",
          "icd11.foundation:1085655586"
        ],
        "synonyms": [
          "ABCD1 deficiency",
          "ALD",
          "Bronze-Schilder disease",
          "Siemerling-Creutzfeldt disease",
          "X-ALD",
          "X-Linked Adrenoleukodystrophy",
          "X-linked ALD",
          "X-linked adrenoleukodystrophy",
          "adrenoleukodystrophy",
          "adrenoleukodystrophy, X-linked",
          "adrenoleukodystrophy, X-linked recessive",
          "adrenomyeloneuropathy, adult",
          "adrenomyeloneuropathy, adult, X-linked recessive",
          "diffuse cerebral sclerosis of Schilder",
          "diffuse sclerosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A peroxisomal disorder resulting in cerebral demyelination, axonal dysfunction in the spinal cord leading to spastic paraplegia, adrenal insufficiency and in some cases testicular insufficiency."
      },
      "child_count": 15,
      "reference_id": "MONDO:0018544"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18561,
      "label": "adrenoleukodystrophy"
    }
  ]
}