DiseaseID 3298
先天性非球形红细胞溶血性贫血
disease
MSH2017_2016_08_12:Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include defic
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Disease: 1Herb: 1Symptom: 6Target: 24Links: 31
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3298
- Core Entity Id
- 59487
- Source Entity Count
- 1
- Preferred Name
- Anemia, Hemolytic, Congenital Nonspherocytic
- Name Cn
- 先天性非球形红细胞溶血性贫血
- Name Pinyin
- Xian Tian Xing Fei Qiu Xing Hong Xi Bao Rong Xue Xing Pin Xue
- Name En
- Anemia, Hemolytic, Congenital Nonspherocytic
- 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; Nutritional and Metabolic Diseases; 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 DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.|CSP2006:group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte; in some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Anemia, Hemolytic, Congenital Nonspherocytic
Role
preferred
Name
Anemia, Nonspherocytic Hemolytic, Due To G6Pd Deficiency
Role
preferred
Name
Hemolytic Anemia, Nonspherocytic, Due To Glucose Phosphate Isomerase Deficiency
Role
preferred
Name
Congenital Nonspherocytic Hemolytic Anemia
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS000149HBDIS019692HBDIS020668
Me Sh
D000746
Omim
300908613470
Umls
C0002882C2720289C3150730
Sym Map
SMDE01020SMDE02542SMDE05849
Do Class
DOID:7
Dis Ge Net
C0002882C2720289C3150730
Umls Sty
T047
Me Sh Class
C15C16C18
Etcm Disease
Anemia, Nonspherocytic Hemolytic, Due to G6pd DeficiencyHemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency
Tcmbank Disease
13869147932315
Itcmdb Generated
ITX-DISEASE-2AC0442B0CEEITX-DISEASE-FD125D919262
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency Details pageDisease Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 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
Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases
Disease Name
Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases
Disease Definition
MSH2017_2016_08_12:Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.|CSP2006:group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte; in some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; 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 DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome