Iatrogenic botulism
General Information (adopted from Orphanet):
Synonyms, Signs: |
Inadvertent botulism |
Number of Symptoms | 11 |
OrphanetNr: | 254509 |
OMIM Id: |
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ICD-10: |
A05.1 |
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: | > 180 cases [Orphanet] |
Inheritance: |
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Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Botulism
-Rare infectious disease -Rare neurologic disease |
Symptom Information:
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(HPO:0000079) | Abnormality of the urinary system | Frequent [Orphanet] | 88 / 7739 | |||
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(HPO:0000615) | Abnormality of the pupil | Very frequent [Orphanet] | 39 / 7739 | |||
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(HPO:0000508) | Ptosis | Very frequent [Orphanet] | 459 / 7739 | |||
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(HPO:0002015) | Dysphagia | Very frequent [Orphanet] | 301 / 7739 | |||
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(HPO:0100021) | Cerebral palsy | Very frequent [Orphanet] | 36 / 7739 | |||
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(HPO:0006824) | Cranial nerve paralysis | Very frequent [Orphanet] | 81 / 7739 | |||
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(HPO:0006597) | Diaphragmatic paralysis | Very frequent [Orphanet] | 16 / 7739 | |||
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(HPO:0002019) | Constipation | Frequent [Orphanet] | 194 / 7739 | |||
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(HPO:0002093) | Respiratory insufficiency | Frequent [Orphanet] | 410 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Very frequent [Orphanet] | 859 / 7739 | |||
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(HPO:0001522) | Death in infancy | Occasional [Orphanet] | 275 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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