Bradykinesia
Symptom Information:
| Symptom ID: | HPO:0002067 | ||||||||
| Synonyms: |
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| Is a (Direct Parents): |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormality of extrapyramidal motor function(HPO:0002071) Bradykinesia(HPO:0002067) MedDRA: Nervous system disorders(MedDRA:10029205) Abnormality of movement(HPO:0100022) Dyskinesias and movement disorders NEC(MedDRA:10013929) Bradykinesia(HPO:0002067) |
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| Database Frequency: | 62 / 7739 | ||||||||
| Resource: |
All diseases associated with this symptom:
| 6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
| Aceruloplasminemia | (Orphanet:48818) |
| Adult polyglucosan body disease | (Orphanet:206583) |
| Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
| Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
| Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
| Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
| Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
| Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
| Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
| BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
| Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
| Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
| CADASIL | (Orphanet:136) |
| Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
| Classical progressive supranuclear palsy | (Orphanet:240071) |
| Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
| Dystonia 16 | (Orphanet:210571) |
| Early-onset parkinsonism - intellectual deficit | (Orphanet:2379) |
| Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
| Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
| HERNS syndrome | (Orphanet:63261) |
| Huntington disease | (Orphanet:399) |
| Huntington disease-like 2 | (Orphanet:98934) |
| Infantile dystonia-parkinsonism | (Orphanet:238455) |
| Juvenile Huntington disease | (Orphanet:248111) |
| Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
| LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
| Leigh syndrome | (Orphanet:506) |
| Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
| MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 2 | (OMIM:615157) |
| Multiple system atrophy | (Orphanet:102) |
| NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2B | (OMIM:610217) |
| NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
| Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
| Neuroferritinopathy | (Orphanet:157846) |
| PARALYSIS AGITANS, JUVENILE, OF HUNT | (OMIM:168100) |
| PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:607688) |
| PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:610297) |
| PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
| PARKINSON DISEASE 17 | (OMIM:614203) |
| PARKINSON DISEASE 18, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:614251) |
| PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE | (OMIM:600116) |
| PARKINSON DISEASE 20, EARLY-ONSET | (OMIM:615530) |
| PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:605909) |
| PARKINSON DISEASE 7, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:606324) |
| PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
| PARKINSON DISEASE, LATE-ONSET | (OMIM:168600) |
| PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
| Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
| Parkinsonian-pyramidal syndrome | (Orphanet:171695) |
| Perry syndrome | (Orphanet:178509) |
| Rapid-onset dystonia-parkinsonism | (Orphanet:71517) |
| SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY | (OMIM:183050) |
| SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
| SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
| Spinocerebellar ataxia type 17 | (Orphanet:98759) |
| Spinocerebellar ataxia type 2 | (Orphanet:98756) |
| Spinocerebellar ataxia type 3 | (Orphanet:98757) |
| Wilson disease | (Orphanet:905) |
| X-linked parkinsonism-spasticity syndrome | (Orphanet:363654) |
| Young adult-onset Parkinsonism | (Orphanet:2828) |