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