Rigidity
Symptom Information:
Symptom ID: | HPO:0002063 | |||||||||||||||||||||
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) Rigidity(HPO:0002063) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle tone abnormalities(MedDRA:10028343) Rigidity(HPO:0002063) |
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Database Frequency: | 92 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
AICARDI-GOUTIERES SYNDROME 6 | (OMIM:615010) |
Aceruloplasminemia | (Orphanet:48818) |
Adult-onset dystonia-parkinsonism | (Orphanet:199351) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Atypical progressive supranuclear palsy | (Orphanet:99750) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 1 | (OMIM:213600) |
Behavioral variant of frontotemporal dementia | (Orphanet:275864) |
Beta-propeller protein-associated neurodegeneration | (Orphanet:329284) |
Bilateral striopallidodentate calcinosis | (Orphanet:1980) |
Biotin-responsive basal ganglia disease | (Orphanet:65284) |
CADASIL | (Orphanet:136) |
CARASIL | (Orphanet:199354) |
CEREBROCORTICAL DEGENERATION OF INFANCY | (OMIM:213950) |
CHOREOATHETOSIS, FAMILIAL INVERTED | (OMIM:118750) |
CLN10 disease | (Orphanet:228337) |
CLN9 disease | (Orphanet:228357) |
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome | (Orphanet:309854) |
Classical phenylketonuria | (Orphanet:79254) |
Classical progressive supranuclear palsy | (Orphanet:240071) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 | (OMIM:616211) |
Familial dementia, British type | (Orphanet:97345) |
Fatal infantile hypertonic myofibrillar myopathy | (Orphanet:280553) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Gerstmann-Straussler-Scheinker syndrome | (Orphanet:356) |
Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency | (Orphanet:284426) |
Glycogen storage disease due to lactate dehydrogenase deficiency | (Orphanet:2364) |
Harlequin ichthyosis | (Orphanet:457) |
Huntington disease | (Orphanet:399) |
Huntington disease-like 1 | (Orphanet:157941) |
Huntington disease-like 2 | (Orphanet:98934) |
Hypomyelination with atrophy of basal ganglia and cerebellum | (Orphanet:139441) |
Infantile dystonia-parkinsonism | (Orphanet:238455) |
Juvenile Huntington disease | (Orphanet:248111) |
Juvenile parkinsonism with intellectual deficit due to DNAJC6 deficiency | (Orphanet:352497) |
King-Denborough syndrome | (Orphanet:99741) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
LUBS X-LINKED MENTAL RETARDATION SYNDROME | (OMIM:300260) |
Malignant hyperthermia | (Orphanet:423) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Menkes disease | (Orphanet:565) |
Multiple system atrophy | (Orphanet:102) |
NEMALINE MYOPATHY 5 | (OMIM:605355) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
Nemaline myopathy | (Orphanet:607) |
Neuroferritinopathy | (Orphanet:157846) |
Niemann-Pick disease type A | (Orphanet:77292) |
OLIVOPONTOCEREBELLAR ATROPHY V | (OMIM:164700) |
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) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Pelizaeus-Merzbacher-like due to GJC2 mutation | (Orphanet:280282) |
Perry syndrome | (Orphanet:178509) |
Progressive supranuclear palsy - parkinsonism | (Orphanet:240085) |
RIGIDITY AND MULTIFOCAL SEIZURE SYNDROME, LETHAL NEONATAL | (OMIM:614498) |
SPINOCEREBELLAR ATAXIA WITH RIGIDITY AND PERIPHERAL NEUROPATHY | (OMIM:183050) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 1 | (OMIM:601104) |
SUPRANUCLEAR PALSY, PROGRESSIVE, 2 | (OMIM:609454) |
Severe neonatal-onset encephalopathy with microcephaly | (Orphanet:209370) |
Spinocerebellar ataxia type 17 | (Orphanet:98759) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Steinert myotonic dystrophy | (Orphanet:273) |
Stiff person syndrome | (Orphanet:3198) |
Thiamine-responsive encephalopathy | (Orphanet:199348) |
Young adult-onset Parkinsonism | (Orphanet:2828) |