spasticity
Basic Information
- Description
- A nervous system symptom that is characterized by an abnormal increase in muscle tone or stiffness of muscle, which might interfere with movement, speech, or be associated with discomfort or pain.
- Identifier
- SYMP_0000141
- Notation
- SYMP:0000141
- Category
- symptoms
Related Diseases
- 3-methylglutaconic aciduria type 3
- 3-methylglutaconic aciduria type 4
- 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome
- Behr syndrome
- Charlevoix-Saguenay spastic ataxia
- De Sanctis-Cacchione syndrome
- Gaucher's disease type IIIC
- Holoprosencephaly 13, X-linked
- Kohlschutter-Tonz syndrome
- Machado-Joseph disease
- Parkinson's disease 19A
- Sjogren-Larsson syndrome
- X-linked mental retardation Gustavson type
- X-linked spinocerebellar ataxia 3
- alpha-methylacyl-CoA racemase deficiency
- amyotrophic lateral sclerosis type 25
- amyotrophic lateral sclerosis-parkinsonism/dementia complex 1
- autosomal dominant distal hereditary motor neuronopathy 2
- autosomal recessive cerebellar ataxia
- autosomal recessive intellectual developmental disorder 18
- autosomal recessive spinocerebellar ataxia 31
- cerebellar ataxia type 42
- complex cortical dysplasia with other brain malformations
- complex cortical dysplasia with other brain malformations 1
- complex cortical dysplasia with other brain malformations 2
- complex cortical dysplasia with other brain malformations 5
- complex cortical dysplasia with other brain malformations 6
- developmental and epileptic encephalopathy 91
- early onset progressive encephalopathy with brain atrophy and thin corpus callosum
- frontotemporal dementia and/or amyotrophic lateral sclerosis 6
- glutamate formiminotransferase deficiency
- hereditary spastic paraplegia
- hereditary spastic paraplegia 12
- hereditary spastic paraplegia 14
- hereditary spastic paraplegia 16
- hereditary spastic paraplegia 17
- hereditary spastic paraplegia 18
- hereditary spastic paraplegia 19
- hereditary spastic paraplegia 25
- hereditary spastic paraplegia 27
- hereditary spastic paraplegia 29
- hereditary spastic paraplegia 30
- hereditary spastic paraplegia 32
- hereditary spastic paraplegia 3A
- hereditary spastic paraplegia 47
- hereditary spastic paraplegia 50
- hereditary spastic paraplegia 52
- hereditary spastic paraplegia 63
- hereditary spastic paraplegia 70
- hereditary spastic paraplegia 72A
- hereditary spastic paraplegia 77
- hereditary spastic paraplegia 79B
- hereditary spastic paraplegia 80
- hereditary spastic paraplegia 89
- hereditary spastic paraplegia 90A
- hypomyelinating leukodystrophy 11
- immunodeficiency 11B
- infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- leukoencephalopathy with vanishing white matter
- megalencephalic leukoencephalopathy with subcortical cysts
- megalencephalic leukoencephalopathy with subcortical cysts 2A
- microlissencephaly
- mitochondrial complex IV deficiency nuclear type 15
- multiple mitochondrial dysfunctions syndrome 3
- neurodegeneration with brain iron accumulation
- neurodegeneration with brain iron accumulation 2b
- neurodegeneration with brain iron accumulation 5
- neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies
- neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
- neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
- neurodevelopmental disorder with midbrain and hindbrain malformations
- neurodevelopmental disorder with spasticity and poor growth
- obsolete Alpers syndrome
- obsolete Jensen syndrome
- pontocerebellar hypoplasia type 16
- pontocerebellar hypoplasia type 2B
- pontocerebellar hypoplasia type 2C
- pontocerebellar hypoplasia type 2D
- pontocerebellar hypoplasia type 2F
- pontocerebellar hypoplasia type 3
- primary autosomal recessive microcephaly 17
- primary progressive multiple sclerosis
- rhizomelic chondrodysplasia punctata type 2
- spinal cord lipoma
- spinocerebellar ataxia type 17
- syndromic microphthalmia 8
Medical Disclaimer: The information provided on this website is for general informational and educational purposes only.
It is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with questions about your medical condition.