Abnormal pyramidal signs
Symptom Information:
Symptom ID: | HPO:0007256 | ||||||||||||||||||||||
Synonyms: |
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Cross references: |
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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) Abnormal pyramidal signs(HPO:0007256) MedDRA: |
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Database Frequency: | 116 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-@METHYLGLUTACONIC ACIDURIA WITH CATARACTS, NEUROLOGIC INVOLVEMENT,AND NEUTROPENIA | (OMIM:616271) |
ALG13-CDG | (Orphanet:324422) |
AMYOTROPHIC LATERAL SCLEROSIS 10 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA | (OMIM:612069) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Adult neuronal ceroid lipofuscinosis | (Orphanet:79262) |
Adult polyglucosan body disease | (Orphanet:206583) |
Adult-onset autosomal dominant leukodystrophy | (Orphanet:99027) |
Alexander disease | (Orphanet:58) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alpha-mannosidosis | (Orphanet:61) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Atypical Gaucher disease due to saposin C deficiency | (Orphanet:309252) |
Atypical progressive supranuclear palsy | (Orphanet:99750) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant spastic paraplegia type 13 | (Orphanet:100994) |
Autosomal dominant spastic paraplegia type 19 | (Orphanet:100999) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
Autosomal recessive ataxia due to ubiquinone deficiency | (Orphanet:139485) |
Autosomal recessive cerebellar ataxia - saccadic intrusion | (Orphanet:95434) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 28 | (Orphanet:101008) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
Behr syndrome | (Orphanet:1239) |
Behçet disease | (Orphanet:117) |
Bilateral frontoparietal polymicrogyria | (Orphanet:101070) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
CADDS | (Orphanet:369942) |
CARASIL | (Orphanet:199354) |
CHOREOATHETOSIS, FAMILIAL INVERTED | (OMIM:118750) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Coats plus syndrome | (Orphanet:313838) |
Cogan syndrome | (Orphanet:1467) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Cystinosis | (Orphanet:213) |
Cystinuria | (Orphanet:214) |
Dentatorubral pallidoluysian atrophy | (Orphanet:101) |
Dihydropyrimidinuria | (Orphanet:38874) |
Dystonia 16 | (Orphanet:210571) |
ENCEPHALOPATHY, PROGRESSIVE, WITH OR WITHOUT LIPODYSTROPHY | (OMIM:615924) |
Ethylmalonic encephalopathy | (Orphanet:51188) |
Free sialic acid storage disease | (Orphanet:834) |
Friedreich ataxia 1 | (OMIM:229300) |
Fucosidosis | (Orphanet:349) |
Gaucher disease type 3 | (Orphanet:77261) |
Giant axonal neuropathy | (Orphanet:643) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Huntington disease-like 3 | (Orphanet:157946) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Hypomyelination - congenital cataract | (Orphanet:85163) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Infantile neuroaxonal dystrophy | (Orphanet:35069) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile neuronal ceroid lipofuscinosis | (Orphanet:79264) |
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS | (OMIM:614561) |
Leukoencephalopathy-palmoplantar keratoderma syndrome | (Orphanet:2386) |
Multiple osteochondromas | (Orphanet:321) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 2A | (OMIM:256600) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Niemann-Pick disease type C | (Orphanet:646) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Oculocerebral hypopigmentation syndrome, Cross type | (Orphanet:2719) |
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
PELIZAEUS-MERZBACHER DISEASE | (OMIM:312080) |
PORENCEPHALY 1 | (OMIM:175780) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Pelizaeus-Merzbacher-like disease | (Orphanet:280270) |
Pelizaeus-Merzbacher-like due to AIMP1 mutation | (Orphanet:280293) |
Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
Polyarteritis nodosa | (Orphanet:767) |
Progressive supranuclear palsy - parkinsonism | (Orphanet:240085) |
Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
Pyruvate dehydrogenase deficiency | (Orphanet:765) |
Refsum disease | (Orphanet:773) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Sandhoff disease | (Orphanet:796) |
Sandhoff disease, adult form | (Orphanet:309169) |
Sandhoff disease, infantile form | (Orphanet:309155) |
Sandhoff disease, juvenile form | (Orphanet:309162) |
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome | (Orphanet:369939) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 10 | (Orphanet:98761) |
Spinocerebellar ataxia type 13 | (Orphanet:98768) |
Spinocerebellar ataxia type 20 | (Orphanet:101110) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |
Spinocerebellar ataxia type 7 | (Orphanet:94147) |
Spinocerebellar ataxia type 8 | (Orphanet:98760) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Tropical spastic paraparesis | (Orphanet:289326) |
Whipple disease | (Orphanet:3452) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked spastic paraplegia type 16 | (Orphanet:100997) |
X-linked spinocerebellar ataxia type 4 | (Orphanet:85292) |
[DEL] SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE | (OMIM:607259) |