Bradykinesia

Symptom Information:

Symptom ID: HPO:0002067
Synonyms:
Bradykinesia (finding) [Orphanet:43320]
Bradykinesia [Orphanet:43320]
Bradykinesia [OMIM:Bradykinesia]
Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia [Orphanet:43320]
Bradykinesia [MedDRA:10006100]
Bradykinesia (in severe cases) [OMIM:Bradykinesia (in severe cases)]
Execution movement disorder [Orphanet:43320]
Quality:
Cross references:
Orphanet:43320 "Execution movement disorder/dysmetria/bradykinesia/akinesia/apraxia" [Orphanet:43320]
OMIM: "Bradykinesia" [OMIM:Bradykinesia]
OMIM: "Bradykinesia (in severe cases)" [OMIM:Bradykinesia (in severe cases)]
UMLS:C0233565 "Bradykinesia" [HPO:0002067]
UMLS:C0233565 "Bradykinesia" [Orphanet:43320]
Is a (Direct Parents):
Orphanet [DEL]Motor deficit/trouble
HPO         Abnormality of extrapyramidal motor function
MedDRA Dyskinesias and movement disorders NEC
Orphanet Dysmetria
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)
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)