Enthesitis-related arthritis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
ERA Juvenile spondylarthropathy |
| Number of Symptoms | 7 |
| OrphanetNr: | 85438 |
| OMIM Id: |
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| ICD-10: |
M08.1 |
| 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: | 5.7 of 100 000 [Orphanet] |
| Inheritance: |
Unknown [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Juvenile idiopathic arthritis
-Rare respiratory disease -Rare systemic or rheumatologic disease Systemic diseases with anterior uveitis -Rare eye disease |
Symptom Information:
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(HPO:0000164) | Abnormality of the teeth | Frequent [Orphanet] | 291 / 7739 | |||
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(HPO:0100533) | Inflammatory abnormality of the eye | Very frequent [Orphanet] | 70 / 7739 | |||
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(HPO:0100769) | Synovitis | Very frequent [Orphanet] | 86 / 7739 | |||
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(HPO:0100773) | Cartilage destruction | Frequent [Orphanet] | 7 / 7739 | |||
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(HPO:0100550) | Tendon rupture | Occasional [Orphanet] | 17 / 7739 | |||
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(HPO:0011227) | Elevated C-reactive protein level | Very frequent [Orphanet] | 55 / 7739 | |||
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(HPO:0100686) | Enthesitis | Frequent [Orphanet] | 5 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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