Orphanet: Secondary polyarteritis nodosa

Search for a rare disease

Other search option(s)

Alphabetical list

Suggest an update

(*) Required fields.

You are (*)

If you have selected the “Other” category, please specify which type of user you are: *

Email address: *

Topic of your comment *

Epidemiology data

Clinical signs

Nomenclature and/or coding

Your message *

(3000 characters remaining)

Attention

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Orphanet doesn't provide personalised answers. To get in touch with the Orphanet team, please contact

Information provided in your contribution (including your email address) will be stocked in .CSV files that will be sent as an email to Orphanet's teams. These emails might be conserved in the teams' mailboxes, in our backoffice servers but will not be registered in our databases (for more information see our section General Data Protection Regulation and data privacy (GDPR) and Confidentiality).

Check this box if you wish to receive a copy of your message

Please reproduce the text below: *

Secondary polyarteritis nodosa

Disease definition

Secondary polyarteritis nodosa (PAN) is a rare serious form of PAN (see this term) characterized by vasculitis in a background of viral infection, primarily with hepatitis B virus (HBV).

ORPHA:439746

Classification level: Subtype of disorder

Synonym(s):
- Secondary PAN
- Secondary periarteritis nodosa
Prevalence: -
Inheritance: Not applicable
Age of onset: -
ICD-10: M30.0 M30.8
ICD-11: 4A44.4
OMIM: -
UMLS: C5680050
MeSH: -
GARD: -
MedDRA: -

A summary on this disease is available in Español (2015) Italiano (2015) Nederlands (2015)

Detailed information

General public

Article for general public
Svenska (2014) - Socialstyrelsen
Arabic (2016) - PRINTO/PRES
Bengali (2016) - PRINTO/PRES
Czech (2016) - PRINTO/PRES
Dansk (2016) - PRINTO/PRES
Deutsch (2016) - PRINTO/PRES
Greek (2016) - PRINTO/PRES
Español (2016) - PRINTO/PRES
Français (2016) - PRINTO/PRES
Hebrew (2016) - PRINTO/PRES
Hrvatski (2016) - PRINTO/PRES
Magyar (2016) - PRINTO/PRES
Italiano (2016) - PRINTO/PRES
Latvian (2016) - PRINTO/PRES
Nederlands (2016) - PRINTO/PRES
Norsk (2016) - PRINTO/PRES
Polski (2016) - PRINTO/PRES
Português (2016) - PRINTO/PRES
Romanian (2016) - PRINTO/PRES
Russian (2016) - PRINTO/PRES
Slovak (2016) - PRINTO/PRES
Slovensko (2016) - PRINTO/PRES
Serbian (2016) - PRINTO/PRES
Thai (2016) - PRINTO/PRES
Türkçe (2016) - PRINTO/PRES
Ukrainian (2016) - PRINTO/PRES
Chinese (2016) - PRINTO/PRES

Guidelines

Clinical practice guidelines
Deutsch (2013) - AWMF
Français (2019) - PNDS
Español (2020, pdf) - Asoc Española de Pediatría
English (2020) - Orphanet J Rare Dis

produced/endorsed by ERN(s) FSMR

produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

Eurordis directory

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.