{
  "id": 18404,
  "label": "neurodegeneration with brain iron accumulation",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018307",
  "properties": {
    "xrefs": [
      "DOID:0110734",
      "GARD:0011899",
      "MEDGEN:444156",
      "MESH:C538421",
      "NANDO:2100241",
      "OMIMPS:234200",
      "Orphanet:385",
      "UMLS:C2931845",
      "icd11.foundation:440483530"
    ],
    "synonyms": [
      "NBIA",
      "neurodegeneration with brain iron accumulation"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Neurodegeneration with brain iron accumulation (NBIA, formerly Hallervorden-Spatz syndrome) encompasses a group of rare neurodegenerative disorders characterized by progressive extrapyramidal dysfunction (dystonia, rigidity, choreoathetosis), iron accumulation in the brain and the presence of axonal spheroids, usually limited to the central nervous system."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 14,
  "parents": [
    {
      "id": 4393,
      "label": "iron metabolism disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2777
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2351",
          "ICD10CM:E83.1",
          "ICD9:275.0",
          "MEDGEN:8438",
          "MESH:D019189",
          "SCTID:30913008",
          "UMLS:C0012715"
        ],
        "synonyms": [
          "disorder of iron metabolism",
          "disorder, iron metabolism",
          "disorders, iron metabolism",
          "iron metabolism disorder",
          "metabolism disorder, iron",
          "metabolism disorders, iron"
        ],
        "definition": "Disorders in the processing of iron in the body: its absorption, transport, storage, and utilization."
      },
      "child_count": 2,
      "reference_id": "MONDO:0002279"
    },
    {
      "id": 4397,
      "label": "neuroaxonal dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2367",
          "MEDGEN:90924",
          "MESH:D019150",
          "NCIT:C161542",
          "SCTID:230365004",
          "UMLS:C0338473"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A nonspecific term referring both to the pathologic finding of swelling of distal portions of axons in the brain and to disorders which feature this finding. Neuroaxonal dystrophy is seen in various genetic diseases, vitamin deficiencies, and aging. Infantile neuroaxonal dystrophy is an autosomal recessive disease characterized by arrested psychomotor development at 6 months to 2 years of age, ataxia, brain stem dysfunction, and quadriparesis. Juvenile and adult forms also occur. Pathologic findings include brain atrophy and widespread accumulation of axonal spheroids throughout the neuroaxis, peripheral nerves, and dental pulp. (From Davis & Robertson, Textbook of Neuropathology, 2nd ed, p927)"
      },
      "child_count": 2,
      "reference_id": "MONDO:0002283"
    },
    {
      "id": 7073,
      "label": "movement disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:480",
          "EFO:0004280",
          "ICD9:333.90",
          "ICD9:333.99",
          "MEDGEN:10113",
          "MESH:D009069",
          "NCIT:C116757",
          "SCTID:60342002",
          "UMLS:C0026650"
        ],
        "synonyms": [
          "movement disease",
          "movement disorder",
          "movement disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement."
      },
      "child_count": 54,
      "reference_id": "MONDO:0005395"
    },
    {
      "id": 16360,
      "label": "hereditary dementia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3823,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020028",
          "MEDGEN:1842422",
          "Orphanet:158124",
          "UMLS:C5680680"
        ],
        "synonyms": [
          "genetic dementia"
        ],
        "definition": "An instance of dementia that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 30,
      "reference_id": "MONDO:0015547"
    },
    {
      "id": 18954,
      "label": "inborn errors of metabolism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6795
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:655",
          "GARD:0022508",
          "MEDGEN:6323",
          "MESH:D008661",
          "MedDRA:10058097",
          "MedDRA:10062018",
          "NANDO:2100159",
          "NCIT:C34816",
          "Orphanet:68367",
          "SCTID:86095007",
          "UMLS:C0025521",
          "icd11.foundation:733825440"
        ],
        "synonyms": [
          "congenital metabolic disorder",
          "congenital metabolism disorder",
          "hereditary metabolic disease",
          "inborn disorders of metabolism",
          "inborn error of metabolism",
          "inborn errors of metabolism",
          "inborn metabolic disorder",
          "inherited disorder of metabolism",
          "inherited disorders of metabolism",
          "inherited metabolic disorder",
          "rare inborn errors of metabolism",
          "rare inherited metabolic disorder",
          "rare metabolic disease"
        ],
        "definition": "An inherited disorder resulting from an enzyme defect in biochemical and metabolic pathways affecting proteins, fats, carbohydrates metabolism or organelle function."
      },
      "child_count": 186,
      "reference_id": "MONDO:0019052"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020280",
          "MEDGEN:1825988",
          "MESH:D020271",
          "NCIT:C97073",
          "Orphanet:183500",
          "UMLS:C5680568"
        ],
        "synonyms": [
          "genetic neurodegenerative disease",
          "hereditary neurodegenerative disease",
          "hereditary neurodegenerative disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by progressive degeneration and atrophy of the nervous system."
      },
      "child_count": 164,
      "reference_id": "MONDO:0024237"
    }
  ],
  "children": [
    {
      "id": 10554,
      "label": "pantothenate kinase-associated neurodegeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3981",
          "GARD:0006564",
          "ICD10CM:G23.0",
          "ICD9:333.0",
          "MEDGEN:6708",
          "MESH:D006211",
          "NANDO:1200534",
          "NANDO:2200886",
          "NCIT:C84988",
          "NORD:1550",
          "OMIM:234200",
          "Orphanet:157850",
          "SCTID:2992000",
          "UMLS:C0018523"
        ],
        "synonyms": [
          "brain iron accumulation type I syndrome",
          "Hallervorden-Spatz disease",
          "Hallervorden-Spatz syndrome",
          "NBIA1",
          "PKAN",
          "neurodegeneration with brain iron accumulation 1",
          "neurodegeneration with brain iron accumulation type 1",
          "pantothenate kinase-associated neurodegeneration",
          "pigmentary pallidal degeneration",
          "Pkan neuroaxonal dystrophy, juvenile-onset",
          "neuroaxonal dystrophy, late infantile"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Pantothenate kinase-associated neurodegeneration (PKAN) is the most common type of neurodegeneration with brain iron accumulation (NBIA), a rare neurodegenerative disorder characterized by progressive extrapyramidal dysfunction (dystonia, rigidity, choreoathetosis), iron accumulation on the brain and axonal spheroids in the central nervous system."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009319"
    },
    {
      "id": 10650,
      "label": "Woodhouse-Sakati syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16526,
        18404,
        23452
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112264",
          "GARD:0005592",
          "ICD9:759.89",
          "MEDGEN:83337",
          "MESH:C536742",
          "OMIM:241080",
          "Orphanet:3464",
          "SCTID:237616002",
          "UMLS:C0342286",
          "icd11.foundation:1893572805"
        ],
        "synonyms": [
          "Woodhouse-Sakati syndrome",
          "diabetes-hypogonadism-deafness-intellectual disability syndrome",
          "woodhouse-Sakati syndrome",
          "extrapyramidal disorder, progressive, with primary hypogonadism, intellectual disability, and alopecia",
          "extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia",
          "hypogonadism, alopecia, diabetes mellitus, intellectual disability, deafness, and extrapyramidal syndrome",
          "hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome",
          "hypogonadism, diabetes mellitus, alopecia, intellectual disability, and electrocardiographic abnormalities",
          "hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic abnormalities",
          "woodhouse Sakati syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Woodhouse-Sakati syndrome is a multisystemic disorder characterized by hypogonadism, alopecia, diabetes mellitus, intellectual deficit and extrapyramidal signs with choreoathetoid movements and dystonia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009419"
    },
    {
      "id": 11634,
      "label": "neurodegeneration with brain iron accumulation 5",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110739",
          "GARD:0012570",
          "MEDGEN:763887",
          "NCIT:C175210",
          "OMIM:300894",
          "Orphanet:329284",
          "SCTID:732959007",
          "UMLS:C3550973"
        ],
        "synonyms": [
          "BPAN",
          "NBIA5",
          "SENDA",
          "WDR45 neurodegeneration with brain iron accumulation",
          "beta-propeller protein-associated neurodegeneration",
          "neurodegeneration with brain iron accumulation 5",
          "neurodegeneration with brain iron accumulation 5, X-linked dominant",
          "neurodegeneration with brain iron accumulation caused by mutation in WDR45",
          "neurodegeneration with brain iron accumulation type 5",
          "static encephalopathy Of childhood with neurodegeneration In adulthood",
          "static encephalopathy of childhood with neurdegeneration in adulthood",
          "neurodegeneration with brain iron accululation 5",
          "static encephalopathy of childhood with neurodegeneration in adulthood"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Beta-propeller protein-associated neurodegeneration (BPAN), also known as static encephalopathy of childhood with neurodegeneration in adulthood, is a rare form of neurodegeneration with brain iron accumulation (NBIA) characterized by early-onset developmental delay and further neurological deterioration in early adulthood."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010476"
    },
    {
      "id": 12531,
      "label": "aceruloplasminemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17107,
        17988,
        18404,
        19000
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050711",
          "GARD:0009499",
          "ICD9:277.6",
          "MEDGEN:168057",
          "NANDO:1200540",
          "NANDO:2200582",
          "NORD:707",
          "OMIM:604290",
          "Orphanet:48818",
          "SCTID:124224004",
          "UMLS:C0878682"
        ],
        "synonyms": [
          "cerebellar ataxia",
          "aceruloplasminemia",
          "hereditary ceruloplasmin deficiency",
          "hypoceruloplasminemia, hereditary",
          "ceruloplasmin deficiency",
          "familial apoceruloplasmin deficiency",
          "hemosiderosis, systemic, due to aceruloplasminemia",
          "hypoceruloplasminemia",
          "systemic hemosiderosis due to aceruloplasminemia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "An adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011426"
    },
    {
      "id": 12733,
      "label": "neuroferritinopathy",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16361,
        17988,
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110737",
          "GARD:0010686",
          "ICD9:333.0",
          "MEDGEN:381211",
          "MESH:C548080",
          "NANDO:1200539",
          "NANDO:1200542",
          "OMIM:606159",
          "Orphanet:157846",
          "SCTID:699299001",
          "UMLS:C1853578"
        ],
        "synonyms": [
          "NBIA3",
          "adult basal ganglia disease",
          "ferritin-related neurodegeneration",
          "hereditary ferritinopathy",
          "neurodegeneration with brain iron accumulation type 3",
          "neuroferritinopathy",
          "basal ganglia disease adult-onset",
          "basal ganglia disease, adult-onset",
          "neurodegeneration with brain iron accumulation 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neuroferritinopathy is a late-onset type of neurodegeneration with brain iron accumulation (NBIA) characterized by progressive chorea or dystonia and subtle cognitive deficits."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011638"
    },
    {
      "id": 12794,
      "label": "Kufor-Rakeb syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3149,
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060556",
          "GARD:0009174",
          "MEDGEN:338281",
          "MESH:C537177",
          "NORD:1959",
          "OMIM:606693",
          "Orphanet:306674",
          "UMLS:C1847640"
        ],
        "synonyms": [
          "Kufor Rakeb Syndrome",
          "Kufor-Rakeb syndrome",
          "PARK9",
          "KRPPD",
          "KRS",
          "Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia",
          "Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia",
          "Parkinson disease 9, autosomal recessive",
          "Parkinson disease 9, autosomal recessive, juvenile-onset",
          "Parkinson disease type 9",
          "ceroid lipofuscinosis, neuronal, 12",
          "park 9"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Kufor-Rakeb syndrome (KRS) is a rare genetic neurodegenerative disorder characterized by juvenile Parkinsonism, pyramidal degeneration (dystonia), supranuclear palsy, and cognitive impairment."
      },
      "child_count": 2,
      "reference_id": "MONDO:0011706"
    },
    {
      "id": 14697,
      "label": "neurodegeneration with brain iron accumulation 4",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110738",
          "GARD:0012569",
          "ICD9:333.0",
          "MEDGEN:482001",
          "NANDO:1200540",
          "NCIT:C175707",
          "OMIM:614298",
          "Orphanet:289560",
          "SCTID:709415008",
          "UMLS:C3280371"
        ],
        "synonyms": [
          "C19orf12 neurodegeneration with brain iron accumulation",
          "MPAN",
          "NBIA due to C19orf12 mutation",
          "NBIA4",
          "mitochondrial Protein-associated neurodegeneration",
          "neurodegeneration with brain iron accumulation 4",
          "neurodegeneration with brain iron accumulation caused by mutation in C19orf12",
          "neurodegeneration with brain iron accumulation due to C19orf12 mutation",
          "neurodegeneration with brain iron accumulation type 4",
          "mitochondrial membrane protein-associated neurodegeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Mitochondrial membrane protein-sssociated neurodegeneration (MPAN), also known as neurogeneration with brain iron accumulation (NBIA) due to C19orf12 mutations, is an autosomal recessive neurodegenerative disorder characterized by iron accumulation in specific regions of the brain, usually the basal ganglia, and associated with slowly progressive pyramidal (spasticity) and extrapyramidal (dystonia) signs, motor axonal neuropathy, optic atrophy, cognitive decline, and neuropsychiatric abnormalities."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013674"
    },
    {
      "id": 15294,
      "label": "neurodegeneration with brain iron accumulation 6",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110740",
          "GARD:0012571",
          "MEDGEN:1387791",
          "OMIM:615643",
          "Orphanet:397725",
          "SCTID:732264002",
          "UMLS:C4517377"
        ],
        "synonyms": [
          "COASY neurodegeneration with brain iron accumulation",
          "CoPAN",
          "NBIA6",
          "neurodegeneration with brain iron accumulation 6",
          "neurodegeneration with brain iron accumulation caused by mutation in COASY",
          "neurodegeneration with brain iron accumulation due to COASY mutation",
          "neurodegeneration with brain iron accumulation type 6",
          "COASY protein-associated neurodegeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "COASY protein-associated neurodegeneration (CoPAN) is a very rare, slowly progressive form of neurodegeneration with brain iron accumulation (NBIA) characterized by classic NBIA features. The clinical manifestations include early-onset spastic-dystonic paraparesis, oromandibular dystonia, dysarthria, parkinsonism, axonal neuropathy, progressive cognitive impairment, complex motor tics, and obsessive-compulsive disorder."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014290"
    },
    {
      "id": 18173,
      "label": "PLA2G6-associated neurodegeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012567",
          "NORD:1302",
          "Orphanet:329303"
        ],
        "synonyms": [
          "PLA2G6 neurodegeneration with brain iron accumulation",
          "PLAN",
          "neurodegeneration with brain iron accumulation caused by mutation in PLA2G6"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any neurodegeneration with brain iron accumulation in which the cause of the disease is a mutation in the PLA2G6 gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:0017998"
    },
    {
      "id": 18174,
      "label": "fatty acid hydroxylase-associated neurodegeneration",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16082,
        16607,
        18270,
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010810",
          "MEDGEN:777150",
          "MESH:C580102",
          "NANDO:1200541",
          "Orphanet:329308",
          "UMLS:C3668943"
        ],
        "synonyms": [
          "FAHN"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Fatty acid hydroxylase-associated neurodegeneration (FAHN) is a very rare, autosomal recessive form of neurodegeneration with brain iron accumulation (NBIA) characterized by childhood-onset focal dystonia, progressive spastic paraplegia that progresses to tetra paresis, ataxia, dysarthria, intellectual decline, and oculomotor disturbances (optic atrophy), accompanied by iron deposition in the globus pallidus."
      },
      "child_count": 0,
      "reference_id": "MONDO:0017999"
    },
    {
      "id": 23381,
      "label": "early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16222,
        18404,
        19713
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017914",
          "MEDGEN:1798874",
          "Orphanet:496756",
          "UMLS:C5567451"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0044651"
    },
    {
      "id": 23616,
      "label": "neurodegeneration with brain iron accumulation 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025969",
          "MEDGEN:1647672",
          "OMIM:617916",
          "UMLS:C4693583"
        ],
        "synonyms": [
          "neurodegeneration with brain iron accumulation 7",
          "NBIA7"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054763"
    },
    {
      "id": 23617,
      "label": "neurodegeneration with brain iron accumulation 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025970",
          "MEDGEN:1645224",
          "OMIM:617917",
          "UMLS:C4693587"
        ],
        "synonyms": [
          "neurodegeneration with brain iron accumulation 8",
          "NBIA8"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0054764"
    },
    {
      "id": 25798,
      "label": "neurodegeneration with brain iron accumulation 9",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026909",
          "MEDGEN:1845761",
          "OMIM:620669",
          "UMLS:C5882740"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0958012"
    }
  ],
  "roots": [
    {
      "id": 4393,
      "label": "iron metabolism disease"
    },
    {
      "id": 4397,
      "label": "neuroaxonal dystrophy"
    },
    {
      "id": 7073,
      "label": "movement disorder"
    },
    {
      "id": 16360,
      "label": "hereditary dementia"
    },
    {
      "id": 18954,
      "label": "inborn errors of metabolism"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    }
  ]
}