Lyme disease
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Lyme borreliosis |
| Number of Symptoms | 26 |
| OrphanetNr: | 91546 |
| OMIM Id: |
|
| ICD-10: |
A69.2 |
| UMLs: |
C0024198 |
| MeSH: |
D008193 |
| MedDRA: |
10025169 |
| Snomed: |
23502006 |
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: |
Infectious disease with peripheral neuropathy
-Rare neurologic disease Rare bacterial infectious disease -Rare infectious disease |
Symptom Information:
|
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(HPO:0000613) | Photophobia | Occasional [Orphanet] | 158 / 7739 | |||
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(HPO:0100576) | Amaurosis fugax | Occasional [Orphanet] | 13 / 7739 | |||
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(HPO:0100533) | Inflammatory abnormality of the eye | Occasional [Orphanet] | 70 / 7739 | |||
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(HPO:0006824) | Cranial nerve paralysis | Frequent [Orphanet] | 81 / 7739 | |||
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(HPO:0100785) | Insomnia | Occasional [Orphanet] | 18 / 7739 | |||
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(HPO:0002354) | Memory impairment | Occasional [Orphanet] | 63 / 7739 | |||
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(HPO:0009830) | Peripheral neuropathy | Occasional [Orphanet] | 206 / 7739 | |||
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(HPO:0002315) | Headache | Occasional [Orphanet] | 175 / 7739 | |||
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(HPO:0000708) | Behavioral abnormality | Occasional [Orphanet] | 212 / 7739 | |||
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(HPO:0002383) | Encephalitis | Occasional [Orphanet] | 41 / 7739 | |||
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(HPO:0001287) | Meningitis | Frequent [Orphanet] | 46 / 7739 | |||
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(HPO:0000763) | Sensory neuropathy | Occasional [Orphanet] | 78 / 7739 | |||
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(HPO:0100769) | Synovitis | Frequent [Orphanet] | 86 / 7739 | |||
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(HPO:0005059) | Arthralgia/arthritis | Frequent [Orphanet] | 141 / 7739 | |||
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(HPO:0002017) | Nausea and vomiting | Occasional [Orphanet] | 134 / 7739 | |||
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(HPO:0008065) | Aplasia/Hypoplasia of the skin | Occasional [Orphanet] | 81 / 7739 | |||
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(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0001031) | Subcutaneous lipoma | Occasional [Orphanet] | 112 / 7739 | |||
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(HPO:0000988) | Skin rash | Occasional [Orphanet] | 98 / 7739 | |||
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(HPO:0011025) | Abnormality of cardiovascular system physiology | Occasional [Orphanet] | 41 / 7739 | |||
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(HPO:0011675) | Arrhythmia | Occasional [Orphanet] | 226 / 7739 | |||
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(HPO:0001945) | Fever | Occasional [Orphanet] | 218 / 7739 | |||
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(HPO:0003326) | Myalgia | Occasional [Orphanet] | 143 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Occasional [Orphanet] | 859 / 7739 | |||
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(MedDRA:10025421) | Macule | Very frequent [Orphanet] | 55 / 7739 | |||
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(HPO:0030350) | Erythematous papule | Frequent [Orphanet] | 123 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|