anemia, hemolytic, congenital nonspherocytic

Preferred Label : anemia, hemolytic, congenital nonspherocytic;

MeSH definition : 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.;

MeSH synonym : anemia, congenital nonspherocytic hemolytic; hemolytic anemia, congenital nonspherocytic; congenital nonspherocytic hemolytic anemia; anemia, hemolytic congenital, nonspherocytic;

MeSH annotation : do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; DF: ANEMIA HEMOL CONGEN NONSPHER;

Details

Origin ID

D000746;

UMLS CUI

C0002882;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Currated CISMeF NLP mapping
- Hereditary nonspherocytic hemolytic anemia (disorder) [SNOMED CT concept]
- congenital nonspherocytic hemolytic anemia [DO Concept]
- congenital nonspherocytic hemolytic anemia [Disease (Nov.)]
- congenital nonspherocytic hemolytic anemia, nos [SNOMED Notion]
DO Cross reference
- congenital nonspherocytic hemolytic anemia [DO Concept]
MeSH Descriptor(s) used for indexing
- glucose-6-phosphate isomerase [MeSH Descriptor]
Record concept(s)
- anemia, hemolytic, congenital nonspherocytic [MeSH concept]
Related MeSH Supplementary Concept(s)
- adenosine triphosphatase deficiency, anemia due to [MeSH Supplementary Concept]
- anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane [MeSH Supplementary Concept]
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH Supplementary Concept]
- pyruvate kinase deficiency of red cells [MeSH Supplementary Concept]
- triosephosphate isomerase deficiency [MeSH Supplementary Concept]
See also
- Triose-Phosphate isomerase [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary nonspherocytic haemolytic anaemia [MedDRA LLT]
- Hereditary nonspherocytic hemolytic anemia [MedDRA LLT]
- Hereditary nonspherocytic hemolytic anemia (disorder) [SNOMED CT concept]
- congenital nonspherocytic hemolytic anemia [DO Concept]
- congenital nonspherocytic hemolytic anemia [Disease (Nov.)]
- congenital nonspherocytic hemolytic anemia, nos [SNOMED Notion]

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