Rigidity

Symptom Information:

Symptom ID: HPO:0002063
Synonyms:
Muscle rigidity [HPO:0002063]
Muscle rigidity [Orphanet:43340]
Muscle rigidity (finding) [Orphanet:43340]
rigidity [HPO:0002063]
Muscle Rigidity [Orphanet:43340]
Muscle rigidity [OMIM:Muscle rigidity]
Rigidity [OMIM:Rigidity]
Hypertonia/spasticity/rigidity/stiffness [Orphanet:43340]
Muscle rigidity [MedDRA:10028330]
Lead pipe rigidity [MedDRA:10028330]
Marked rigidity [MedDRA:10028330]
Muscular rigidity spastic [MedDRA:10028330]
Plastic rigidity [MedDRA:10028330]
Rigidity [MedDRA:10028330]
Rigidity bodily [MedDRA:10028330]
Rigidity muscle [MedDRA:10028330]
Rigidity of limbs [MedDRA:10028330]
Muscular rigor [MedDRA:10028330]
Rigidity (juvenile form) [OMIM:Rigidity (juvenile form)]
Rigidity (later) [OMIM:Rigidity (later)]
Rigidity (uncommon) [OMIM:Rigidity (uncommon)]
Quality:
Cross references:
Orphanet:43340 "Hypertonia/spasticity/rigidity/stiffness" [Orphanet:43340]
OMIM: "Muscle rigidity" [OMIM:Muscle rigidity]
OMIM: "Rigidity" [OMIM:Rigidity]
OMIM: "Rigidity (juvenile form)" [OMIM:Rigidity (juvenile form)]
OMIM: "Rigidity (later)" [OMIM:Rigidity (later)]
OMIM: "Rigidity (uncommon)" [OMIM:Rigidity (uncommon)]
UMLS:C0700109 "rigidity" [HPO:0002063]
UMLS:C0026837 "Muscle Rigidity" [Orphanet:43340]
Is a (Direct Parents):
Orphanet Spasticity
Orphanet [DEL]Motor deficit/trouble
MedDRA Muscle tone abnormalities
HPO         Abnormality of central 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)
                Rigidity(HPO:0002063)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Muscle disorders(MedDRA:10028302)
       Muscle tone abnormalities(MedDRA:10028343)
          Rigidity(HPO:0002063)
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)