01
Diseases
Anemia, Hemolytic, Congenital Nonspherocytic
anemia, hemolytic, congenital nonspherocytic
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 6
Basic Information
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Core Information
- Disease Name
- Anemia, Hemolytic, Congenital Nonspherocytic
- Standard Disease Name
- anemia, hemolytic, congenital nonspherocytic
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- D000746
- OMIM ID
- MTHU039166
- UMLS ID
- C0002882
- HPO ID
- No data
Description and Extensions
- Description
- 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.
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Related Targets
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