ORPHA:439746
Secondary polyarteritis nodosa
Synonyms: Secondary PAN · Secondary periarteritis nodosa
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Secondary polyarteritis nodosa (PAN) is a rare serious form of PAN characterized by vasculitis in a background of viral infection, primarily with hepatitis B virus (HBV).
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Secondary polyarteritis nodosa | Secondary PAN · Secondary periarteritis nodosa |
| fr | Périartérite noueuse secondaire | PAN secondaire · Polyartérite noueuse secondaire |
| de | Sekundäre Polyarteriitis nodosa | Periarteriitis nodosa, sekundäre · Sekundäre PAN |
| es | Poliarteritis nodosa secundaria | PAN secundaria · Periarteritis nodosa secundaria |
| it | Poliarterite nodosa secondaria | PAN secondaria · Periarterite nodosa secondaria |
| nl | Secundaire polyarteriitis nodosa | Secundaire PAN · Secundaire periarteriitis nodosa |
| pt | Poliarterite nodosa secundária | |
| pl | Wtórne guzkowe zapalenie tętnic | Secondary periarteritis nodosa · Wtórne PAN |
| cs | Sekundární polyarteritis nodosa | Sekundární PAN · Sekundární periarteritis nodosa |
| uk | Вторинний вузликовий поліартеріїт | Вторинна PAN · Вторинний вузликовий периартеріїт |
| zh | 继发性结节性多动脉炎 | 继发性结节性动脉周围炎 |
| tr | Sekonder poliarteritis nodoza | Sekonder PAN · Sekonder periarterit nodosa |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M30.0 | NTBT | attributed | validated |
| ICD-10 | M30.8 | NTBT | attributed | validated |
| ICD-11 | 4A44.4 | NTBT | attributed | validated |
| MONDO | 0018594 | E | validated | |
| UMLS | C5680050 | 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 (1):
- ORPHA:767Polyarteritis nodosa
rare neurological diseases; rare renal diseases; rare systemic and rheumatological diseases; rare circulatory system diseases; rare systemic or rheumatologic diseases of childhood; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/439746
- This record as JSON: /data/d/439746.json