DiseaseID 4172
血红蛋白病
disease
Hemoglobin C - beta-thalassemia (HbC - BT) is a form of beta-thalassemia (see this term) resulting in moderate hemolytic anemia.
Relationship Network
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Disease: 1Herb: 1Symptom: 2Target: 24Links: 27
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4172
- Core Entity Id
- 60480
- Source Entity Count
- 1
- Preferred Name
- Hemoglobinopathies
- Name Cn
- 血红蛋白病
- Name Pinyin
- Xue Hong Dan Bai Bing
- Name En
- Hemoglobinopathies
- 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 Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- Hemoglobin C - beta-thalassemia (HbC - BT) is a form of beta-thalassemia (see this term) resulting in moderate hemolytic anemia.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hemoglobinopathies
Role
preferred
Name
Hemoglobin C Disease
Role
preferred
Name
Hemoglobin C-Beta-Thalassemia Syndrome
Role
preferred
Name
Hemoglobin D Disease
Role
preferred
Name
Hemoglobin E Disease
Role
preferred
Name
Hemoglobinopathy
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001304HBDIS001308HBDIS005130HBDIS006711
Me Sh
D006445D006453
Umls
C0019021C0019045
Icd10
D58.2
Sym Map
SMDE00506SMDE09327SMDE09330
Do Class
DOID:7
Dis Ge Net
C0019021C0019045C0238159C0272080
Orphanet
231242
Umls Sty
T047
Me Sh Class
C15C16
Etcm Disease
Hemoglobin C-Beta-Thalassemia Syndrome
Tcmbank Disease
115661170516097599
Itcmdb Generated
ITX-DISEASE-37069A30267AITX-DISEASE-ED881671BE74
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Hemoglobin C-Beta-Thalassemia Syndrome Details page
Do Class Name
disease of anatomical entity
Disease Type
diseasegroup
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hemoglobin C-Beta-Thalassemia Syndrome
Global Category
Rare diseases
Anatomical Category
Blood diseases
Disease Definition
Hemoglobin C - beta-thalassemia (HbC - BT) is a form of beta-thalassemia (see this term) resulting in moderate hemolytic anemia.NCI2016_02D:An autosomal recessive hemoglobinopathy with a mild clinical course. Most patients are asymptomatic. When symptoms appear, they include mild hemolytic anemia and occasionally jaundice.|MSH2017_2016_08_12:A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.NCI2016_02D:An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.|MSH2017_2016_08_12:A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.|CSP2006:group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
diseasegroup
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome