{
  "id": 24681,
  "label": "leukodystrophy, demyelinating, adult-onset, autosomal dominant, atypical",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0700286",
  "properties": {
    "xrefs": [
      "DOID:0051014",
      "GARD:0027379",
      "MEDGEN:1875111",
      "OMIM:621061",
      "UMLS:C5975581"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9523,
      "label": "adult-onset autosomal dominant demyelinating leukodystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17371,
        20345,
        26194
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DECIPHER:59",
          "DOID:0051015",
          "DOID:0060785",
          "GARD:0010587",
          "MEDGEN:356995",
          "MESH:C566813",
          "OMIMPS:169500",
          "Orphanet:99027",
          "SCTID:448054001",
          "UMLS:C1868512"
        ],
        "synonyms": [
          "ADLD",
          "adult-onset autosomal dominant demyelinating leukodystrophy",
          "adult-onset autosomal dominant leukodystrophy",
          "leukodystrophy, adult-onset, autosomal dominant",
          "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type",
          "Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type, formerly",
          "autosomal dominant adult-onset demyelinating leukodystrophy",
          "autosomal dominant leukodystrophy with autonomic disease",
          "leukodystrophy, demyelinating, ADULT-onset, autosomal dominant",
          "multiple sclerosis-like disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, slowly progressive neurological disorder involving central nervous system demyelination, leading to autonomic dysfunction, ataxia and mild cognitive impairment."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008215"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9523,
      "label": "adult-onset autosomal dominant demyelinating leukodystrophy"
    }
  ]
}