Parkinsonism

Symptom Information:

Symptom ID: HPO:0001300
Synonyms:
Parkinsonian disease [HPO:0001300]
Parkinsonism [OMIM:Parkinsonism]
Parkinsonism (in some patients) [OMIM:Parkinsonism (in some patients)]
Parkinsonism (in some) [OMIM:Parkinsonism (in some)]
Parkinsonism (later onset) [OMIM:Parkinsonism (later onset)]
Parkinsonism (later) [OMIM:Parkinsonism (later)]
Parkinsonism (less common) [OMIM:Parkinsonism (less common)]
Parkinsonism [MedDRA:10034010]
Quality:
Cross references:
OMIM: "Parkinsonism" [OMIM:Parkinsonism]
OMIM: "Parkinsonism (in some patients)" [OMIM:Parkinsonism (in some patients)]
OMIM: "Parkinsonism (in some)" [OMIM:Parkinsonism (in some)]
OMIM: "Parkinsonism (later onset)" [OMIM:Parkinsonism (later onset)]
OMIM: "Parkinsonism (later)" [OMIM:Parkinsonism (later)]
OMIM: "Parkinsonism (less common)" [OMIM:Parkinsonism (less common)]
UMLS:C0242422 "Parkinsonism" [HPO:0001300]
Is a (Direct Parents):
MedDRA Parkinson's disease and parkinsonism
HPO         Abnormality of extrapyramidal motor function
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)
                   Parkinsonism(HPO:0001300)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Parkinson's disease and parkinsonism(MedDRA:10034005)
          Parkinsonism(HPO:0001300)
Database Frequency: 75 / 7739
Resource:

All diseases associated with this symptom:

6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
ALZHEIMER DISEASE (OMIM:104300)
ALZHEIMER DISEASE 2 (OMIM:104310)
ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL (OMIM:502500)
Adult-onset dystonia-parkinsonism (Orphanet:199351)
Amyotrophic lateral sclerosis-parkinsonism-dementia complex (Orphanet:90020)
Atypical progressive supranuclear palsy (Orphanet:99750)
Autosomal dominant dopa-responsive dystonia (Orphanet:98808)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal recessive dopa-responsive dystonia (Orphanet:101150)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 4 (OMIM:615007)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 (OMIM:615483)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
CADASIL (Orphanet:136)
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM (OMIM:118301)
CLN3 disease (Orphanet:228346)
CLN4B disease (Orphanet:228343)
Choreoacanthocytosis (Orphanet:2388)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Classical progressive supranuclear palsy (Orphanet:240071)
DEMENTIA, LEWY BODY (OMIM:127750)
DEMENTIA/PARKINSONISM WITH NON-ALZHEIMER AMYLOID PLAQUES (OMIM:125320)
Dystonia 16 (Orphanet:210571)
Early-onset autosomal dominant Alzheimer disease (Orphanet:1020)
Early-onset parkinsonism - intellectual deficit (Orphanet:2379)
FRONTOTEMPORAL DEMENTIA (OMIM:600274)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105550)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 2 (OMIM:615911)
Fragile X-associated tremor/ataxia syndrome (Orphanet:93256)
Frontotemporal dementia with motor neuron disease (Orphanet:275872)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Infantile dystonia-parkinsonism (Orphanet:238455)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency (Orphanet:352497)
Kufor-Rakeb syndrome (Orphanet:306674)
Leber plus disease (Orphanet:99718)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Multiple system atrophy (Orphanet:102)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Neuroferritinopathy (Orphanet:157846)
PARALYSIS AGITANS, JUVENILE, OF HUNT (OMIM:168100)
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 4, AUTOSOMAL DOMINANT (OMIM:605543)
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:605909)
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT (OMIM:607060)
PARKINSON DISEASE, LATE-ONSET (OMIM:168600)
PRESENILIN 1 (OMIM:104311)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Parkinsonian-pyramidal syndrome (Orphanet:171695)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Perry syndrome (Orphanet:178509)
Progressive non-fluent aphasia (Orphanet:100070)
Progressive supranuclear palsy - parkinsonism (Orphanet:240085)
Rapid-onset dystonia-parkinsonism (Orphanet:71517)
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 (OMIM:601104)
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 (OMIM:609454)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 17 (Orphanet:98759)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Spinocerebellar ataxia type 28 (Orphanet:101109)
Spinocerebellar ataxia type 3 (Orphanet:98757)
X-linked parkinsonism-spasticity syndrome (Orphanet:363654)
Young adult-onset Parkinsonism (Orphanet:2828)