DiseaseID 5026
风湿性紫癜
disease
100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.
Relationship Network
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Disease: 1Experiment: 1Symptom: 12Target: 23Links: 37
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5026
- Core Entity Id
- 61464
- Source Entity Count
- 1
- Preferred Name
- Rheumatoid Purpura
- Name Cn
- 风湿性紫癜
- Name Pinyin
- Feng Shi Xing Zi Dian
- Name En
- Rheumatoid Purpura
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Cardiovascular Diseases; Immune System DiseasesCardiovascular Diseases; Immune System Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and SymptomsHemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and SymptomsRespiratory Tract Diseases; Male Urogenital Diseases; Immune System Diseases; Female Urogenital Diseases and Pregnancy Complications
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the immune system; Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Respiratory Tract Diseases; Immune System DiseasesHemic and Lymphatic DiseasesImmune System Diseases; Cardiovascular DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
- Hpo Class Name
- Abnormality of the immune system; Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entity
- Disease Definition
- 100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Rheumatoid Purpura
Role
preferred
Name
Anti-Glomerular Basement Membrane Disease
Role
preferred
Name
Autoimmune Thrombocytopenia
Role
preferred
Name
Purpura Rheumatoid
Role
preferred
Name
Vasculitis, Leukocytoclastic, Cutaneous
Role
preferred
Name
Chronic Idiopathic Thrombocytopenic Purpura
Role
preferred
Name
Henoch-Schoenlein Purpura
Role
preferred
Name
Idiopathic Thrombocytopenia
Role
preferred
Name
Immune Thrombocytopenic Purpura
Role
preferred
Name
Purpura Hemorrhagica
Role
preferred
Name
Purpura, Nonthrombocytopenic
Role
preferred
Name
Thrombocytopenia Due To Platelet Alloimmunization
Role
preferred
Name
Thrombocytopenia, Cyclic
Role
preferred
Name
Vasculitis, Hemorrhagic
Role
preferred
Name
Allergic Purpura
Role
alias
Name
Autoimmune Thrombocytopenic Purpura
Role
alias
Name
Goodpasture Syndrome
Role
alias
Name
Hypersensitivity Angiitis
Role
alias
Name
Hypersensitivity Vasculitis
Role
alias
Name
Idiopathic Thrombocytopenic Purpura
Role
alias
Name
Immune Thrombocytopenia
Role
alias
Name
Purpura, Immune Thrombocytopenic
Role
alias
Name
Purpura, Schoenlein-Henoch
Role
alias
Name
Purpura, Thrombocytopenic, Idiopathic
Role
alias
Name
Thrombocytopenic Purpura, Autoimmune
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001973
Herb
HBDIS002549HBDIS003091HBDIS003436HBDIS003542HBDIS005429HBDIS005440HBDIS006751HBDIS006753HBDIS006755HBDIS008563HBDIS008802HBDIS008893HBDIS012419
Me Sh
D011695D016553D018366D019867
Omim
188020188030233450
Umls
C0034152C0086922C0151436C0242584C0398650C0403529
Icd10
D69.0D69.3M31.0
Med Dra
10021245
Sym Map
SMDE02576SMDE05953SMDE06203SMDE09357SMDE12617SMDE14222
Do Class
DOID:7
Dis Ge Net
C0034152C0042386C0086922C0151436C0242461C0242584C0272282C0272286C0272293C0376362C0398650C0403529C0920163
Orphanet
3002
Umls Sty
T047
Hpo Class
HP:0001871HP:0002715
Me Sh Class
C08C12C13C14C15C20C23
Etcm Disease
Henoch-Schoenlein Purpura
Tcmbank Disease
13245151051851018738210462350927544321453241066597945883789819773
Itcmdb Generated
ITX-DISEASE-1912A906726CITX-DISEASE-42D80E011BEFITX-DISEASE-64D92685210BITX-DISEASE-7C8C586AD74D
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Henoch-Schoenlein Purpura Details page
Do Class Name
disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the immune system; Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the immune system; Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Henoch-Schoenlein Purpura
Global Category
Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Cardiovascular diseases;Immune diseases;Nephrological diseases;Respiratory diseases
Disease Definition
100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.HPO2016_07_04:The presence of thrombocytopenia in combination with detection of antiplatelet antibodies. [DDD:wouwehand]NCI2016_02D:An autoimmune disorder characterized by the production of autoantibodies against type IV collagen of the glomerular basement membrane of the kidney. In the majority of patients the immune reaction also extends to the alveolar capillary membrane of the lungs. The latter cases are referred to as Goodpasture Syndrome.|NCI2016_02D:An autoimmune disorder characterized by pulmonary hemorrhage and glomerulonephritis. It is a hypersensitivity reaction resulting in the formation of antibodies against the pulmonary alveoli and the basement membrane of the glomeruli.|MSH2017_2016_08_12:An autoimmune disease of the KIDNEY and the LUNG. It is characterized by the presence of circulating autoantibodies targeting the epitopes in the non-collagenous domains of COLLAGEN TYPE IV in the basement membranes of kidney glomeruli (KIDNEY GLOMERULUS) and lung alveoli (PULMONARY ALVEOLI), and the subsequent destruction of these basement membranes. Clinical features include pulmonary alveolar hemorrhage and glomerulonephritis.|CSP2006:combination of pulmonary hemorrhage and glomerulonephritis; known also as the lung purpura glomerulonephritis complex; considered by some to be a form of hypersensitivity reaction.NCI2016_NICHD_1602D:A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin A deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.|NCI2016_02D:A systemic, usually self-limited immune complex vasculitis, characterized by immunoglobulin A deposition in the small vessels and kidneys. It is manifested with small hemorrhages in the skin, gastrointestinal symptoms, arthritis, and nephropathy.|MSH2017_2016_08_12:A systemic non-thrombocytopenic purpura caused by HYPERSENSITIVITY VASCULITIS and deposition of IGA-containing IMMUNE COMPLEXES within the blood vessels throughout the body, including those in the kidney (KIDNEY GLOMERULUS). Clinical symptoms include URTICARIA; ERYTHEMA; ARTHRITIS; GASTROINTESTINAL HEMORRHAGE; and renal involvement. Most cases are seen in children after acute upper respiratory infections.SNOMEDCT_US_2016_09_01:A small-vessel vasculitis presenting with palpable purpura and urticarial lesions which predate the purpuric lesions most frequently observed on the legs. Systemic symptoms including fever, cough, hemoptysis, sinusitis, arthralgia, arthritis, myalgia, abdominal pain, diarrhea, hematochezia, paresthesia, weakness, and hematuria may be observed. Can be idiopathic (up to 50% of cases) or secondary to infection, medications (such as antituberculosis medication), collagen vascular diseases, or neoplasms.|SNOMEDCT_US_2016_09_01:A small-vessel vasculitis presenting with palpable purpura and urticarial lesions which predate the purpuric lesions most frequently observed on the legs. Systemic symptoms including fever, cough, haemoptysis, sinusitis, arthralgia, arthritis, myalgia, abdominal pain, diarrhoea, haematochezia, paraesthesia, weakness, and haematuria may be observed. Can be idiopathic (up to 50% of cases) or secondary to infection, medications (such as antituberculosis medication), collagen vascular diseases, or neoplasms.|MSH2017_2016_08_12:Disorder characterized by a vasculitic syndrome associated with exposure to an antigen such as a drug, infectious agent, or other foreign or endogenous substance. Its pathophysiology includes immune complex deposition and a wide range of skin lesions. Hypersensitivity or allergy is present in some but not all cases.
Me Sh Disease Class
Cardiovascular Diseases; Immune System DiseasesCardiovascular Diseases; Immune System Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and SymptomsHemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and SymptomsRespiratory Tract Diseases; Male Urogenital Diseases; Immune System Diseases; Female Urogenital Diseases and Pregnancy Complications
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Respiratory Tract Diseases; Immune System DiseasesHemic and Lymphatic DiseasesImmune System Diseases; Cardiovascular DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Disease or Syndrome