Abnormality of extrapyramidal motor function
Symptom Information:
Symptom ID: | HPO:0002071 | ||||||||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||||||||||
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) |