ORPHA:91546
Lyme disease
Synonyms: Lyme borreliosis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Lyme disease (named after the towns in the USA where the disease was first identified) is a bacterial infection caused by <i>Borrelia burgdorferi</i>.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Lyme disease | Lyme borreliosis |
| fr | Maladie de Lyme | Borréliose de Lyme |
| de | Lyme-Krankheit | Lyme-Borreliose |
| es | Fiebre de Lyme | Borreliosis de Lyme |
| it | Malattia di Lyme | Borreliosi di Lyme |
| nl | Ziekte van Lyme | Lyme-borreliose |
| pt | Doença de Lyme | |
| pl | Choroba z Lyme | Borelioza z Lyme |
| cs | Lymeská nemoc | Lymeská borelióza |
| uk | Хвороба Лайма | Лайм-бореліоз |
| zh | 莱姆病 | 兰姆氏包柔螺旋体病 |
| tr | Lyme hastalığı | Lyme borelyozu |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | A69.2 | E | specific | validated |
| ICD-11 | 1C1G | E | specific | validated |
| MONDO | 0019632 | E | validated | |
| MeSH | D008193 | E | validated | |
| UMLS | C0024198 | E | validated | |
| MedDRA | 10025169 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:206613Infectious disease with peripheral neuropathy
rare neurological diseases - ORPHA:163582Rare bacterial infectious disease
rare infectious diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
7 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | >1 / 1000 | 177.5 / 100 000 | Europe | Value and class | Validated | [EXPERT] |
| Annual incidence | 1-5 / 10 000 | 16.6 / 100 000 | France | Value and class | Validated | [EXPERT] |
| Annual incidence | 1-5 / 10 000 | 21.9 / 100 000 | Worldwide | Value and class | Not yet validated | emedicine[OTHER] |
| Annual incidence | 1-5 / 10 000 | 12.37 / 100 000 | Hungary | Value and class | Validated | 23428090[PMID] |
| Annual incidence | 1-5 / 10 000 | 36 / 100 000 | Sweden | Value and class | Not yet validated | ORPHANET |
| Annual incidence | >1 / 1000 | 100 / 100 000 | United States | Value and class | Validated | 24045727[PMID] |
| Point prevalence | Unknown | — | Europe | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
24 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Frequent (79-30%) | ||
| HP:0001369 | Arthritis | |
| HP:0006824 | Cranial nerve paralysis | |
| HP:0001386 | Joint swelling | |
| HP:0001287 | Meningitis | |
| Occasional (29-5%) | ||
| HP:0100576 | Amaurosis fugax | |
| HP:0011675 | Arrhythmia | |
| HP:0002829 | Arthralgia | |
| HP:0001678 | Atrioventricular block | |
| HP:0000708 | Atypical behavior | |
| HP:0004334 | Dermal atrophy | |
| HP:0012378 | Fatigue | |
| HP:0001945 | Fever | |
| HP:0002315 | Headache | |
| HP:0002383 | Infectious encephalitis | |
| HP:0100785 | Insomnia | |
| HP:0002354 | Memory impairment | |
| HP:0001324 | Muscle weakness | |
| HP:0003326 | Myalgia | |
| HP:0002017 | Nausea and vomiting | |
| HP:0003401 | Paresthesia | |
| HP:0009830 | Peripheral neuropathy | |
| HP:0000613 | Photophobia | |
| HP:0200036 | Skin nodule | |
| HP:0000554 | Uveitis | |
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/91546
- This record as JSON: /data/d/91546.json