{
  "id": 8652,
  "label": "basal ganglia calcification, idiopathic, childhood-onset",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007247",
  "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"
      }
    ]
  },
  "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": 18799,
      "label": "Aicardi-Goutieres syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5658,
        7611,
        18952,
        21247,
        25666
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050629",
          "GARD:0000575",
          "ICD9:333.0",
          "MEDGEN:97953",
          "MESH:C535607",
          "NANDO:1200996",
          "NANDO:2100244",
          "NANDO:2200893",
          "NORD:111728",
          "OMIMPS:225750",
          "Orphanet:51",
          "SCTID:230312006",
          "UMLS:C0393591"
        ],
        "synonyms": [
          "Aicardi Goutieres syndrome",
          "Aicardi-Goutières Syndrome",
          "Cree encephalitis",
          "encephalopathy with basal ganglia calcification",
          "encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid",
          "AGS",
          "Aicardi-Goutières syndrome",
          "encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis",
          "pseudotoxoplasmosis syndrome"
        ],
        "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"
          }
        ],
        "definition": "Aicardi-Goutieres syndrome (AGS) is an inherited, subacute encephalopathy characterized by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis."
      },
      "child_count": 50,
      "reference_id": "MONDO:0018866"
    },
    {
      "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": 18799,
      "label": "Aicardi-Goutieres syndrome"
    },
    {
      "id": 24405,
      "label": "idiopathic disease"
    }
  ]
}