DiseaseID 5510
嗜酸性粒细胞增多-肌痛综合征
disease
MSH2017_2016_08_12:A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA,
Relationship Network
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Disease: 1Symptom: 4Target: 7Links: 11
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5510
- Core Entity Id
- 62024
- Source Entity Count
- 1
- Preferred Name
- Eosinophilia-Myalgia Syndrome
- Name Cn
- 嗜酸性粒细胞增多-肌痛综合征
- Name Pinyin
- Shi Suan Xing Li Xi Bao Zeng Duo - Ji Tong Zong He Zheng
- Name En
- Eosinophilia-Myalgia Syndrome
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Hemic and Lymphatic Diseases; Nervous System Diseases; Musculoskeletal Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Musculoskeletal Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Eosinophilia-Myalgia Syndrome
Role
preferred
Name
Eosinophilia-Myalgia Syndrome, L-Tryptophan-Related
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS003256HBDIS011387
Me Sh
D016603
Umls
C0085179
Sym Map
SMDE08328
Do Class
DOID:7
Dis Ge Net
C0085179C0751622
Umls Sty
T047
Me Sh Class
C05C10C15
Tcmbank Disease
116022145
Itcmdb Generated
ITX-DISEASE-E0AC503F650D
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A complex systemic syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart. Diagnostic features generally include EOSINOPHILIA, myalgia severe enough to limit usual activities of daily living, and the absence of coexisting infectious, autoimmune or other conditions that may induce eosinophilia. Biopsy of affected tissue reveals a microangiopathy associated with diffuse inflammation involving connective tissue. (From Spitzer et al., J Rheumatol Suppl 1996 Oct;46:73-9; Blackburn WD, Semin Arthritis Rheum 1997 Jun;26(6):788-93)
Me Sh Disease Class
Hemic and Lymphatic Diseases; Nervous System Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Musculoskeletal Diseases; Nervous System Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome