DiseaseID 5203
遗传性球形红细胞增多症
disease
NCI2016_02D:An autosomal dominant inherited disorder characterized by the presence of smaller than normal, sphere-shaped erythrocytes. It results in hemolytic anemia and splenomegaly.|MSH2017_2016_08_12:A group of famili
Relationship Network
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Disease: 1Formula: 10Herb: 2Symptom: 2Target: 23Links: 38
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5203
- Core Entity Id
- 61665
- Source Entity Count
- 1
- Preferred Name
- Hereditary Spherocytosis
- Name Cn
- 遗传性球形红细胞增多症
- Name Pinyin
- Yi Chuan Xing Qiu Xing Hong Xi Bao Zeng Duo Zheng
- Name En
- Hereditary Spherocytosis
- 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 DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:An autosomal dominant inherited disorder characterized by the presence of smaller than normal, sphere-shaped erythrocytes. It results in hemolytic anemia and splenomegaly.|MSH2017_2016_08_12:A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.|CSP2006:autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hereditary Spherocytosis
Role
preferred
Name
Anemia, Hereditary Spherocytic Hemolytic
Role
preferred
Name
Spherocytosis, Hereditary
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS002799HBDIS004651
Me Sh
D013103
Umls
C0037889
Icd10
D58.0
Sym Map
SMDE09437
Do Class
DOID:7
Dis Ge Net
C0037889C0221409
Umls Sty
T047
Me Sh Class
C15C16C23
Etcm Disease
Hereditary Spherocytosis
Tcmbank Disease
136699472
Itcmdb Generated
ITX-DISEASE-72E84E7B7AA1
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease Hereditary Spherocytosis Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hereditary Spherocytosis
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
NCI2016_02D:An autosomal dominant inherited disorder characterized by the presence of smaller than normal, sphere-shaped erythrocytes. It results in hemolytic anemia and splenomegaly.|MSH2017_2016_08_12:A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.|CSP2006:autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome