{
  "id": 18867,
  "label": "XK-related neurodegenerative disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018945",
  "properties": {
    "xrefs": [
      "DOID:0112107",
      "GARD:0010731",
      "ICD9:289.89",
      "MEDGEN:140765",
      "MESH:C564038",
      "NANDO:1200015",
      "OMIM:300842",
      "Orphanet:59306",
      "SCTID:234411007",
      "UMLS:C0398568",
      "icd11.foundation:1749275115"
    ],
    "synonyms": [
      "MLS",
      "McLeod neuroacanthocytosis syndrome",
      "McLeod syndrome",
      "X-linked McLeod syndrome",
      "XK disease",
      "MCLDS"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17399,
      "label": "neuroacanthocytosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7073,
        16361
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050765",
          "GARD:0010902",
          "MESH:D054546",
          "NANDO:1200013",
          "NCIT:C84926",
          "NORD:1501",
          "Orphanet:263440",
          "icd11.foundation:1012724153"
        ],
        "synonyms": [
          "neuroacanthocytosis syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neuroacanthocytosis (NA) syndromes are a group of genetic diseases characterized by the association of red blood cell acanthocytosis (deformed erythrocytes with spike-like protrusions) and progressive degeneration of the basal ganglia."
      },
      "child_count": 4,
      "reference_id": "MONDO:0016987"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17399,
      "label": "neuroacanthocytosis"
    }
  ]
}