DiseaseID 3296
溶血性贫血
disease
MSH2017_2016_08_12:Acquired anemia due to destruction of red blood cells by physical trauma such as FIBRIN strands in the blood vessels, artificial heart valve, AORTIC COARCTATION. I can also be associated with hematolog
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Disease: 1Symptom: 12Target: 24Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3296
- Core Entity Id
- 59485
- Source Entity Count
- 1
- Preferred Name
- Anemia, Hemolytic
- Name Cn
- 溶血性贫血
- Name Pinyin
- Rong Xue Xing Pin Xue
- Name En
- Anemia, Hemolytic
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of blood and blood-forming tissues
- Mesh Class Name
- Hemic and Lymphatic Diseases
- Hpo Class Name
- Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Acquired anemia due to destruction of red blood cells by physical trauma such as FIBRIN strands in the blood vessels, artificial heart valve, AORTIC COARCTATION. I can also be associated with hematologic diseases such as DISSEMINATED INTRAVASCULAR COAGULATION; HEMOLYTIC-UREMIC SYNDROME; and THROMBOTIC THROMBOCYTOPENIC PURPURA.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Anemia, Hemolytic
Role
preferred
Name
Adenylate Kinase Deficiency, Hemolytic Anemia Due To
Role
preferred
Name
Microangiopathic Hemolytic Anemia
Role
preferred
Name
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
Role
preferred
Name
Anemia, Hemolytic, Acquired
Role
preferred
Name
Anemia, Microangiopathic
Role
preferred
Name
Acquired Haemolytic Anaemia
Role
alias
Name
Acquired Haemolytic Anaemia, Unspecified
Role
alias
Name
HEMOLYTIC ANEMIA DUE TO P5N DEFICIENCY
Role
alias
Name
HEMOLYTIC ANEMIA DUE TO UMPH1 DEFICIENCY
Role
alias
Name
Haemolytic Anaemia
Role
alias
Name
Haemolytic Anaemias
Role
alias
Name
Hemolytic Anemia
Role
alias
Name
Increased Hemolysis
Role
alias
Name
P5N DEFICIENCY
Role
alias
Name
PYRIMIDINE 5-PRIME NUCLEOTIDASE DEFICIENCY, HEMOLYTIC ANEMIA DUE TO
Role
alias
Name
UMPH1 DEFICIENCY
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001878HP:0001937
Herb
HBDIS000145HBDIS000146HBDIS000154HBDIS004555HBDIS019371HBDIS028884
Me Sh
D000743
Omim
266120612631
Umls
C0002878C0221021C1849507C2675459
Icd10
D59D59.4D59.9
Sym Map
SMDE01019SMDE01249SMDE05847SMDE10971
Do Class
DOID:7
Dis Ge Net
C0002878C0002879C0002889C0221021C1849507C2675459
Umls Sty
T047
Hpo Class
HP:0001871
Me Sh Class
C15C16
Etcm Disease
Adenylate Kinase Deficiency, Hemolytic Anemia Due to
Tcmbank Disease
12821867819858251313445614787
Itcmdb Generated
ITX-DISEASE-27DAEC73B6E0ITX-DISEASE-7864B7788DBCITX-DISEASE-7E9594C0F7CFITX-DISEASE-97CF5455A8CDITX-DISEASE-AD7687DD03C9
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Adenylate Kinase Deficiency, Hemolytic Anemia Due to Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of blood and blood-forming tissues
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Adenylate Kinase Deficiency, Hemolytic Anemia Due to
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases
Disease Definition
MSH2017_2016_08_12:Acquired anemia due to destruction of red blood cells by physical trauma such as FIBRIN strands in the blood vessels, artificial heart valve, AORTIC COARCTATION. I can also be associated with hematologic diseases such as DISSEMINATED INTRAVASCULAR COAGULATION; HEMOLYTIC-UREMIC SYNDROME; and THROMBOTIC THROMBOCYTOPENIC PURPURA.NCI2016_02D:Anemia resulting from the premature destruction of the peripheral blood red cells. It may be congenital or it may be caused by infections, medications, or malignancies.|MSH2017_2016_08_12:A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES).|HPO2016_07_04:A type of anemia caused by premature destruction of red blood cells (hemolysis). [HPO:probinson]|CSP2006:due to premature destruction of erythrocytes in the spleen or peripheral vessels; commonly associated with glucose-6-phosphate dehydrogenase deficiencies, splenomegaly, and malarial or other infections.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesHemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome