DiseaseID 13184
全身型幼年慢性关节炎
disease
NCI2016_NICHD_1602D:A category of juvenile idiopathic arthritis defined by the presence of arthritis and high fevers, and accompanied by at least 2 of the following systemic features: lymphadenopathy, organomegaly, rash,
Relationship Network
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Disease: 1Experiment: 1Symptom: 7Target: 12Links: 20
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13184
- Core Entity Id
- 70787
- Source Entity Count
- 1
- Preferred Name
- Systemic Onset Juvenile Chronic Arthritis
- Name Cn
- 全身型幼年慢性关节炎
- Name Pinyin
- Quan Shen Xing You Nian Man Xing Guan Jie Yan
- Name En
- Systemic Onset Juvenile Chronic Arthritis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Immune System Diseases; Musculoskeletal Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_NICHD_1602D:A category of juvenile idiopathic arthritis defined by the presence of arthritis and high fevers, and accompanied by at least 2 of the following systemic features: lymphadenopathy, organomegaly, rash, or serositis. Macrophage activation syndrome is a well known complication.|NCI2016_02D:A category of juvenile idiopathic arthritis defined by the presence of arthritis and high fevers, and accompanied by at least 2 of the following systemic features: lymphadenopathy, organomegaly, rash, or serositis. Macrophage activation syndrome is a well known complication.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Systemic Onset Juvenile Chronic Arthritis
Role
preferred
Name
Systemic-Onset Juvenile Idiopathic Arthritis
Role
preferred
Name
Juvenile Arthritis With Systemic Onset
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS014093
Umls
C0087031C1384600
Icd10
M08.2M08.20
Sym Map
SMDE04951SMDE13780
Dis Ge Net
C1384600
Orphanet
85414
Umls Sty
T047
Me Sh Class
C05C17C20
Tcmbank Disease
118312655
Itcmdb Generated
ITX-DISEASE-56E5FFA95F70
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:A category of juvenile idiopathic arthritis defined by the presence of arthritis and high fevers, and accompanied by at least 2 of the following systemic features: lymphadenopathy, organomegaly, rash, or serositis. Macrophage activation syndrome is a well known complication.|NCI2016_02D:A category of juvenile idiopathic arthritis defined by the presence of arthritis and high fevers, and accompanied by at least 2 of the following systemic features: lymphadenopathy, organomegaly, rash, or serositis. Macrophage activation syndrome is a well known complication.Systemic-onset juvenile idiopathic arthritis is marked by the severity of the extra-articular manifestations (fever, cutaneous eruptions) and by an equal sex ratio.
Me Sh Disease Class
Skin and Connective Tissue Diseases; Immune System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
Umls Semantic Type Name
Disease or Syndrome