DiseaseID 3304
镰状细胞贫血
disease
CSP2006:broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Experiment: 5Symptom: 12Target: 12Links: 29
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3304
- Core Entity Id
- 59494
- Source Entity Count
- 1
- Preferred Name
- Anemia, Sickle Cell
- Name Cn
- 镰状细胞贫血
- Name Pinyin
- Lian Zhuang Xi Bao Pin Xue
- Name En
- Anemia, Sickle Cell
- 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; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- CSP2006:broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Anemia, Sickle Cell
Role
preferred
Name
Hemoglobin Sc Disease
Role
preferred
Name
Hemoglobin Ss Disease With Crisis
Role
preferred
Name
Sickle Cell Anemia
Role
preferred
Name
Sickle Cell Disease
Role
alias
Name
Sickle-Cell Anaemia With Crisis
Role
alias
Name
Sickle-Cell Disorders
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS000160HBDIS001307HBDIS005173
Me Sh
D000755D006450
Omim
603903
Umls
C0002895C0019034C0238425
Icd10
D57D57.0D57.00D57.1D57.2D57.20
Med Dra
10040641
Sym Map
SMDE03765SMDE09328SMDE09329
Do Class
DOID:630DOID:7
Dis Ge Net
C0002895C0019034C0238425
Orphanet
232
Umls Sty
T047
Me Sh Class
C15C16
Tcmbank Disease
115381956525198
Itcmdb Generated
ITX-DISEASE-4D36832D4117
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Disease Definition
CSP2006:broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis.NCI2016_02D:A hemoglobinopathy that is considered a hybrid of sickle cell disease and hemoglobin C disease. Patients present with the symptoms of sickle cell disease but the latter are less frequent and severe compared to sickle cell disease.|MSH2017_2016_08_12:One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sick
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome