Neurogenic thoracic outlet syndrome
General Information (adopted from Orphanet):
Synonyms, Signs: |
NTOS Neurogenic costoclavicular syndrome Neurogenic TOS Neurogenic cervical rib syndrome Neurogenic thoracic outlet compression syndrome |
Number of Symptoms | 8 |
OrphanetNr: | 100073 |
OMIM Id: |
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ICD-10: |
G54.0 |
UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Thoracic outlet syndrome
-Rare surgical thoracic disease |
Symptom Information:
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(HPO:0003474) | Sensory impairment | Very frequent [Orphanet] | 54 / 7739 | |||
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(HPO:0000763) | Sensory neuropathy | Very frequent [Orphanet] | 78 / 7739 | |||
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(HPO:0011442) | Abnormality of central motor function | Occasional [Orphanet] | 76 / 7739 | |||
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(HPO:0005059) | Arthralgia/arthritis | Very frequent [Orphanet] | 141 / 7739 | |||
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(HPO:0000772) | Abnormality of the ribs | Frequent [Orphanet] | 146 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Occasional [Orphanet] | 859 / 7739 | |||
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(HPO:0003457) | EMG abnormality | Very frequent [Orphanet] | 78 / 7739 | |||
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(HPO:0003326) | Myalgia | Very frequent [Orphanet] | 143 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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