{
  "id": 21484,
  "label": "basal ganglia calcification, idiopathic, 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024538",
  "properties": {
    "xrefs": [
      "GARD:0025419",
      "MEDGEN:1637664",
      "MESH:C537657",
      "NANDO:1200208",
      "NCIT:C129973",
      "OMIM:213600",
      "OMIM:606656",
      "UMLS:C4551624"
    ],
    "synonyms": [
      "IBGC1",
      "IBGC2",
      "basal ganglia calcification, idiopathic, 1",
      "basal ganglia calcification, idiopathic, 2",
      "basal ganglia calcification, idiopathic, type 1",
      "idiopathic basal ganglia calcification 1",
      "Fahr disease, familial",
      "Fahr disease, familial, formerly",
      "basal ganglia calcification, idiopathic, 3",
      "basal ganglia calcification, idiopathic, 3, formerly",
      "cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset",
      "ferrocalcinosis, cerebrovascular",
      "striopallidodentate calcinosis, autosomal dominant, adult-onset",
      "striopallidodentate calcinosis, bilateral"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10207,
      "label": "bilateral striopallidodentate calcinosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5849,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060230",
          "GARD:0006406",
          "HP:0002135",
          "ICD9:333.0",
          "ICD9:348.89",
          "MESH:C536275",
          "MedDRA:10059626",
          "NANDO:1200207",
          "NORD:1127",
          "OMIMPS:213600",
          "Orphanet:1980",
          "SCTID:110997000",
          "SCTID:230311004",
          "icd11.foundation:1081370436"
        ],
        "synonyms": [
          "BSPDC",
          "PFBC",
          "Primary Familial Brain Calcification",
          "basal ganglia calcification",
          "basal ganglia degeneration with calcification",
          "cerebrovascular ferrocalcinosis",
          "primary familial brain calcification",
          "Fahr disease",
          "idiopathic basal ganglia calcification",
          "basal ganglia calcification, idiopathic"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A basal ganglia disease characterized by the accumulation of calcium deposits in different brain regions, particularly the basal ganglia and dentate nucleus, and is often associated with neurodegeneration."
      },
      "child_count": 20,
      "reference_id": "MONDO:0008947"
    },
    {
      "id": 24405,
      "label": "idiopathic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29381
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:548250",
          "UMLS:C0277553"
        ],
        "synonyms": [
          "idiopathic disorder"
        ],
        "definition": "A disease or disorder for which the cause is of uncertain or unknown."
      },
      "child_count": 79,
      "reference_id": "MONDO:0700007"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10207,
      "label": "bilateral striopallidodentate calcinosis"
    },
    {
      "id": 24405,
      "label": "idiopathic disease"
    }
  ]
}