DiseaseID 16733
显微镜下多血管炎
disease
NCI2016_NICHD_1602D:Systemic vasculitis affecting small vessels that is necrotizing and non-granulomatous, with little to no immune complex deposition. Clinically it is characterized by involvement of the kidneys, skin,
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Disease: 1Symptom: 12Target: 9Links: 21
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 16733
- Core Entity Id
- 74849
- Source Entity Count
- 1
- Preferred Name
- Microscopic Polyarteritis
- Name Cn
- 显微镜下多血管炎
- Name Pinyin
- Xian Wei Jing Xia Duo Xue Guan Yan
- Name En
- Microscopic Polyarteritis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Immune System Diseases; Nervous System Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_NICHD_1602D:Systemic vasculitis affecting small vessels that is necrotizing and non-granulomatous, with little to no immune complex deposition. Clinically it is characterized by involvement of the kidneys, skin, lung, and peripheral nerves. Antineutrophil cytoplasmic antibody (anti-myeloperoxidase (anti-MPO)) is positive in most cases.|NCI2016_02D:A systemic necrotizing vasculitis that typically affects the small and medium-sized muscular arteries. In some cases, however, microscopic vessels are also affected (e.g., in the kidneys), a condition that has been called microscopic polyarteritis or polyangiitis; this disorder is felt to be more closely associated with Wegener granulomatosis than to classic polyarteritis nodosa.|MSH2017_2016_08_12:A primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Microscopic Polyarteritis
Role
preferred
Name
Microscopic Polyangiitis
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS019076
Me Sh
D055953
Umls
C2347126
Icd10
M31.7
Sym Map
SMDE10985
Dis Ge Net
C2347126
Umls Sty
T047
Me Sh Class
C10C14C20
Tcmbank Disease
26500
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:Systemic vasculitis affecting small vessels that is necrotizing and non-granulomatous, with little to no immune complex deposition. Clinically it is characterized by involvement of the kidneys, skin, lung, and peripheral nerves. Antineutrophil cytoplasmic antibody (anti-myeloperoxidase (anti-MPO)) is positive in most cases.|NCI2016_02D:A systemic necrotizing vasculitis that typically affects the small and medium-sized muscular arteries. In some cases, however, microscopic vessels are also affected (e.g., in the kidneys), a condition that has been called microscopic polyarteritis or polyangiitis; this disorder is felt to be more closely associated with Wegener granulomatosis than to classic polyarteritis nodosa.|MSH2017_2016_08_12:A primary systemic vasculitis of small- and some medium-sized vessels. It is characterized by a tropism for kidneys and lungs, positive association with anti-neutrophil cytoplasmic antibodies (ANCA), and a paucity of immunoglobulin deposits in vessel walls.
Me Sh Disease Class
Cardiovascular Diseases; Immune System Diseases; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome