hyperreflexia
Basic Information
- Identifier
- SYMP_0000058
- Notation
- SYMP:0000058
- Category
- symptoms
Related Diseases
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- Huntington's disease-like 2
- Parkinson's disease 19A
- X-linked monogenic disease
- amyotrophic lateral sclerosis type 22
- autosomal dominant distal hereditary motor neuronopathy 2
- autosomal recessive distal hereditary motor neuronopathy
- cerebellar ataxia type 42
- cerebrotendinous xanthomatosis
- dominant optic atrophy plus syndrome
- hereditary spastic paraplegia 10
- hereditary spastic paraplegia 13
- hereditary spastic paraplegia 14
- hereditary spastic paraplegia 19
- hereditary spastic paraplegia 24
- hereditary spastic paraplegia 29
- hereditary spastic paraplegia 33
- hereditary spastic paraplegia 36
- hereditary spastic paraplegia 3A
- hereditary spastic paraplegia 4
- hereditary spastic paraplegia 41
- hereditary spastic paraplegia 48
- hereditary spastic paraplegia 53
- hereditary spastic paraplegia 55
- hereditary spastic paraplegia 57
- hereditary spastic paraplegia 6
- hereditary spastic paraplegia 61
- hereditary spastic paraplegia 72A
- hereditary spastic paraplegia 73
- hereditary spastic paraplegia 75
- hereditary spastic paraplegia 8
- hereditary spastic paraplegia 82
- hereditary spastic paraplegia 84
- hereditary spastic paraplegia 85
- hereditary spastic paraplegia 86
- hereditary spastic paraplegia 88
- hereditary spastic paraplegia 89
- hereditary spastic paraplegia 90A
- hereditary spastic paraplegia 9A
- hyperekplexia 1
- multiple congenital anomalies-hypotonia-seizures syndrome 2
- multiple congenital anomalies-hypotonia-seizures syndrome 3
- obsolete hereditary spastic paraplegia 1
- obsolete peripheral dysostosis
- primary hypomagnesemia
- spinocerebellar ataxia type 13
- spinocerebellar ataxia type 14
- spinocerebellar ataxia type 23
- spinocerebellar ataxia type 28
- spinocerebellar ataxia type 35
- spinocerebellar ataxia type 36
- syndromic X-linked intellectual disability Claes-Jensen type
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