{
  "id": 10207,
  "label": "bilateral striopallidodentate calcinosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008947",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 10,
  "parents": [
    {
      "id": 5849,
      "label": "basal ganglia disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "CSP:2057-3403",
          "DOID:679",
          "EFO:0009533",
          "ICD9:333.0",
          "MEDGEN:1619147",
          "MESH:D001480",
          "SCTID:70835005",
          "UMLS:C4520981"
        ],
        "synonyms": [
          "basal ganglia disease",
          "collection of basal ganglia disease",
          "collection of basal ganglia disease or disorder",
          "disease of basal ganglia",
          "disease of collection of basal ganglia",
          "disease or disorder of collection of basal ganglia",
          "disorder of collection of basal ganglia",
          "disorder of basal ganglia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease involving the basal ganglia."
      },
      "child_count": 4,
      "reference_id": "MONDO:0003996"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [
    {
      "id": 8652,
      "label": "basal ganglia calcification, idiopathic, childhood-onset",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        18799,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009598",
          "MEDGEN:396262",
          "MESH:C536276",
          "OMIM:114100",
          "UMLS:C1861967"
        ],
        "synonyms": [
          "basal ganglia calcification, idiopathic, childhood-onset",
          "IBGC childhood onset",
          "IBGC, childhood-onset",
          "bilateral striopallidodentate calcinosis childhood-onset",
          "cerebral calcification nonarteriosclerotic idiopathic childhood-onset",
          "cerebral calcification, nonarteriosclerotic, idiopathic, childhood-onset",
          "idiopathic basal ganglia calcification childhood-onset",
          "striopallidodentate calcinosis, bilateral, childhood-onset"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0007247"
    },
    {
      "id": 15014,
      "label": "basal ganglia calcification, idiopathic, 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015893",
          "MEDGEN:767235",
          "OMIM:615007",
          "UMLS:C3554321"
        ],
        "synonyms": [
          "basal ganglia calcification, idiopathic, 4",
          "basal ganglia calcification, idiopathic, type 4",
          "IBGC4"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014004"
    },
    {
      "id": 15210,
      "label": "basal ganglia calcification, idiopathic, 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015973",
          "MEDGEN:815975",
          "OMIM:615483",
          "UMLS:C3809645"
        ],
        "synonyms": [
          "basal ganglia calcification, idiopathic, 5",
          "basal ganglia calcification, idiopathic, type 5",
          "IBGC5"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0014204"
    },
    {
      "id": 15624,
      "label": "basal ganglia calcification, idiopathic, 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016107",
          "MEDGEN:901404",
          "OMIM:616413",
          "UMLS:C4225335"
        ],
        "synonyms": [
          "XPR1 bilateral striopallidodentate calcinosis",
          "basal ganglia calcification, idiopathic, 6",
          "basal ganglia calcification, idiopathic, type 6",
          "bilateral striopallidodentate calcinosis caused by mutation in XPR1",
          "IBGC6"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any bilateral striopallidodentate calcinosis in which the cause of the disease is a mutation in the XPR1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014628"
    },
    {
      "id": 21484,
      "label": "basal ganglia calcification, idiopathic, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0024538"
    },
    {
      "id": 22352,
      "label": "basal ganglia calcification, idiopathic, 7, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025719",
          "MEDGEN:1683911",
          "OMIM:618317",
          "UMLS:C5193025"
        ],
        "synonyms": [
          "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 7, AUTOSOMAL RECESSIVE",
          "IBGC7"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032673"
    },
    {
      "id": 22589,
      "label": "basal ganglia calcification, idiopathic, 8, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016384",
          "MEDGEN:1713414",
          "OMIM:618824",
          "UMLS:C5394199"
        ],
        "synonyms": [
          "BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE",
          "IBGC8"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0032938"
    },
    {
      "id": 25965,
      "label": "basal ganglia calcification, idiopathic, 9, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027078",
          "MEDGEN:1854926",
          "OMIM:620786",
          "UMLS:C5935607"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0968977"
    },
    {
      "id": 26148,
      "label": "basal ganglia calcification, idiopathic, 10, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027334",
          "MEDGEN:1875062",
          "OMIM:621018",
          "UMLS:C5975532"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0975875"
    },
    {
      "id": 26384,
      "label": "basal ganglia calcification, idiopathic, 11, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10207
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "OMIM:621452"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0980939"
    }
  ],
  "roots": [
    {
      "id": 5849,
      "label": "basal ganglia disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}