Abnormality of extrapyramidal motor function

Symptom Information:

Symptom ID: HPO:0002071
Synonyms:
Extrapyramidal dysfunction [HPO:0002071]
Extrapyramidal signs [HPO:0002071]
Extrapyramidal symptoms [HPO:0002071]
Extrapyramidal syndrome [HPO:0002071]
Extrapyramidal tract signs [HPO:0002071]
Extrapyramidal symptoms [Orphanet:43300]
Extrapyramidal disease (disorder) [Orphanet:43300]
Extrapyramidal sign (finding) [Orphanet:43300]
Extrapyramidal sign [Orphanet:43300]
Extrapyramidal Disorders [Orphanet:43300]
Extrapyramidal dysfunction [OMIM:Extrapyramidal dysfunction]
Extrapyramidal signs [OMIM:Extrapyramidal signs]
Extrapyramidal symptoms [OMIM:Extrapyramidal symptoms]
Extrapyramidal syndrome [OMIM:Extrapyramidal syndrome]
Extrapyramidal syndrome [Orphanet:43300]
Extrapyramidal disorder [Orphanet:43300]
Extrapyramidal disorder [MedDRA:10015832]
Benign shuddering attacks [MedDRA:10015832]
Drug-induced extrapyramidal side effects [MedDRA:10015832]
Extrapyramidal disorder (NOS) [MedDRA:10015832]
Extrapyramidal disorder NEC [MedDRA:10015832]
Extrapyramidal symptoms [MedDRA:10015832]
Extrapyramidal syndrome [MedDRA:10015832]
Extrapyramidal syndrome (NOS) [MedDRA:10015832]
Other and unspecified extrapyramidal diseases and abnormal movement disorders [MedDRA:10015832]
Other extrapyramidal disease and abnormal movement disorders [MedDRA:10015832]
Other extrapyramidal diseases and abnormal movement disorders [MedDRA:10015832]
Syndrome extrapyramidal [MedDRA:10015832]
Unspecified extrapyramidal disease and abnormal movement disorder [MedDRA:10015832]
Extrapyramidal disorder aggravate [MedDRA:10015832]
Extrapyramidal disorder aggravated [MedDRA:10015832]
Extrapyramidal signs (in 1 patient) [OMIM:Extrapyramidal signs (in 1 patient)]
Extrapyramidal signs (less common) [OMIM:Extrapyramidal signs (less common)]
Extrapyramidal symptoms (later-onset) [OMIM:Extrapyramidal symptoms (later-onset)]
Quality:
Cross references:
Orphanet:43300 "Extrapyramidal syndrome" [Orphanet:43300]
OMIM: "Extrapyramidal dysfunction" [OMIM:Extrapyramidal dysfunction]
OMIM: "Extrapyramidal signs" [OMIM:Extrapyramidal signs]
OMIM: "Extrapyramidal symptoms" [OMIM:Extrapyramidal symptoms]
OMIM: "Extrapyramidal syndrome" [OMIM:Extrapyramidal syndrome]
OMIM: "Extrapyramidal signs (in 1 patient)" [OMIM:Extrapyramidal signs (in 1 patient)]
OMIM: "Extrapyramidal signs (less common)" [OMIM:Extrapyramidal signs (less common)]
OMIM: "Extrapyramidal symptoms (later-onset)" [OMIM:Extrapyramidal symptoms (later-onset)]
UMLS:C0234133 "Extrapyramidal sign" [Orphanet:43300]
UMLS:C0015371 "Extrapyramidal Disorders" [Orphanet:43300]
Is a (Direct Parents):
HPO         Abnormality of central motor function
MedDRA Dyskinesias and movement disorders NEC
Orphanet [DEL]Motor deficit/trouble
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)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Abnormality of movement(HPO:0100022)
       Dyskinesias and movement disorders NEC(MedDRA:10013929)
          Abnormality of extrapyramidal motor function(HPO:0002071)
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA (OMIM:616271)
3-methylglutaconic aciduria type 3 (Orphanet:67047)
6-pyruvoyl-tetrahydropterin synthase deficiency (Orphanet:13)
AICARDI-GOUTIERES SYNDROME 1 (OMIM:225750)
ALG13-CDG (Orphanet:324422)
ALZHEIMER DISEASE 3 (OMIM:607822)
Aceruloplasminemia (Orphanet:48818)
Adenylosuccinate lyase deficiency (Orphanet:46)
Adult neuronal ceroid lipofuscinosis (Orphanet:79262)
Adult polyglucosan body disease (Orphanet:206583)
Adult-onset dystonia-parkinsonism (Orphanet:199351)
Aicardi-Goutières syndrome (Orphanet:51)
Attenuated Chédiak-Higashi syndrome (Orphanet:352723)
Autosomal dominant optic atrophy and cataract (Orphanet:67036)
Autosomal recessive dopa-responsive dystonia (Orphanet:101150)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 (OMIM:213600)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET (OMIM:114100)
Beta-propeller protein-associated neurodegeneration (Orphanet:329284)
CADASIL (Orphanet:136)
CARASIL (Orphanet:199354)
CLN13 disease (Orphanet:352709)
CLN3 disease (Orphanet:228346)
CLN4A disease (Orphanet:228340)
CLN4B disease (Orphanet:228343)
Cerebrotendinous xanthomatosis (Orphanet:909)
Chédiak-Higashi syndrome (Orphanet:167)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Coats plus syndrome (Orphanet:313838)
Cystinuria (Orphanet:214)
Ethylmalonic encephalopathy (Orphanet:51188)
FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 1 (OMIM:105550)
Familial encephalopathy with neuroserpin inclusion bodies (Orphanet:85110)
Familial melanoma (Orphanet:618)
Gaucher disease (Orphanet:355)
Gerstmann-Straussler-Scheinker syndrome (Orphanet:356)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Huntington disease-like 3 (Orphanet:157946)
Juvenile neuronal ceroid lipofuscinosis (Orphanet:79264)
Kufor-Rakeb syndrome (Orphanet:306674)
L-2-hydroxyglutaric aciduria (Orphanet:79314)
LESCH-NYHAN SYNDROME (OMIM:300322)
LEUKODYSTROPHY, HYPOMYELINATING, 9 (OMIM:616140)
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS (OMIM:614561)
Lesch-Nyhan syndrome (Orphanet:510)
MEGDEL syndrome (Orphanet:352328)
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 4 (OMIM:615159)
MYOPATHY WITH EXTRAPYRAMIDAL SIGNS (OMIM:615673)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Neurodegeneration with brain iron accumulation (Orphanet:385)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
Neuroferritinopathy (Orphanet:157846)
OLIVOPONTOCEREBELLAR ATROPHY V (OMIM:164700)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET (OMIM:260300)
Pantothenate kinase-associated neurodegeneration (Orphanet:157850)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Perry syndrome (Orphanet:178509)
Polyarteritis nodosa (Orphanet:767)
Posterior cortical atrophy (Orphanet:54247)
Primary orthostatic tremor (Orphanet:238606)
Progressive myoclonic epilepsy with dystonia (Orphanet:352596)
SPASTIC PARAPLEGIA WITH ASSOCIATED EXTRAPYRAMIDAL SIGNS (OMIM:182800)
SPINOCEREBELLAR ATAXIA, X-LINKED 2 (OMIM:302600)
SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS (OMIM:271322)
Spastic paraplegia type 2 (Orphanet:99015)
Spinocerebellar ataxia type 1 (Orphanet:98755)
Spinocerebellar ataxia type 10 (Orphanet:98761)
Spinocerebellar ataxia type 21 (Orphanet:98773)
Spinocerebellar ataxia type 3 (Orphanet:98757)
Spinocerebellar ataxia type 7 (Orphanet:94147)
Williams syndrome (Orphanet:904)
Wilson disease (Orphanet:905)
Woodhouse-Sakati syndrome (Orphanet:3464)
Xeroderma pigmentosum (Orphanet:910)