Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Systemic-onset juvenile idiopathic arthritis
Synonyms

Still disease

Systemic-onset JIA

Definitions

A rare pediatric rheumatological disease characterized by the variable occurrence of chronic arthritis, intermittent high spiking fever, maculopapular rash during fever episodes, hepatomegaly and/or splenomegaly, lymphadenopathy, and serositis.

ID

http://www.orpha.net/ORDO/Orphanet_85414

alternative_term

Still disease

Systemic-onset JIA

definition

A rare pediatric rheumatological disease characterized by the variable occurrence of chronic arthritis, intermittent high spiking fever, maculopapular rash during fever episodes, hepatomegaly and/or splenomegaly, lymphadenopathy, and serositis.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=85414

has_age_of_onset

Childhood

has_inheritance

Multigenic/multifactorial

Unknown

hasDbXref

ICD-10:M08.2

OMIM:618795

OMIM:604302

ICD-11:FA24.4

MedDRA:10042061

UMLS:C0087031

label

Systemic-onset juvenile idiopathic arthritis

notation

ORPHA:85414

part_of

http://www.orpha.net/ORDO/Orphanet_92

prefixIRI

ORDO:Orphanet_85414

prefLabel

Systemic-onset juvenile idiopathic arthritis

present_in

Worldwide AND has_point_prevalence_average_value : 3.1 AND has_point_prevalence_range : 1-9 / 100 000

Worldwide AND has_annual_incidence_average_value : 0.6 AND has_annual_incidence_range : 1-9 / 1 000 000

treeView

http://www.orpha.net/ORDO/Orphanet_92

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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