anemia, hemolytic, congenital

Preferred Label : anemia, hemolytic, congenital;

MeSH definition : Hemolytic anemia due to various intrinsic defects of the erythrocyte.;

MeSH synonym : hemolytic anemias, hereditary; hereditary hemolytic anemias; anemia, congenital hemolytic; anemia, hemolytic, hereditary; hemolytic anemia, hereditary; congenital hemolytic anemia; hereditary hemolytic anemia; anemia, hereditary hemolytic; hemolytic anemias, congenital; anemias, hereditary hemolytic; hemolytic anemia, congenital; congenital hemolytic anemias; anemias, congenital hemolytic;

Details

Origin ID

D000745;

UMLS CUI

C0002881;

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]
Automatic exact mappings (from CISMeF team)
- Other hereditary haemolytic anaemias [ICD-10 category (who)]
Currated CISMeF NLP mapping
- Congenital haemolytic anaemia [MedDRA LLT]
- Congenital haemolytic anaemia [Bloc CIM-11]
- Congenital haemolytic anaemia NOS [MedDRA LLT]
- Congenital hemolytic anemia [HPO term]
- Congenital hemolytic anemia [MedDRA LLT]
- Congenital hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary Hemolytic Anemia [NCIt concept]
- Hereditary haemolytic anaemia [ICD-11 Category]
- Hereditary haemolytic anaemia [MedDRA Preferred Term]
- Hereditary haemolytic anaemia NOS [MedDRA LLT]
- Hereditary haemolytic anaemias [MedDRA LLT]
- Hereditary hemolytic anemia [MedDRA LLT]
- Hereditary hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary hemolytic anemia, unspecified [ICD-9 code]
- Hereditary hemolytic anemia, unspecified [ICD-10 Sub-category]
- Hereditary hemolytic anemias [ICD-9 code]
- Hereditary hemolytic anemias [MedDRA LLT]
- congenital hemolytic anemia [DO Concept]
- congenital hemolytic anemia [Disease (Nov.)]
- congenital hemolytic anemia, nos [SNOMED Notion]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]
DO Cross reference
- congenital hemolytic anemia [DO Concept]
HPO term
- Congenital hemolytic anemia [HPO term]
Indexing information
- mitapivat [MeSH Supplementary Concept]
MeSH Descriptor(s) used for indexing
- anemia, hemolytic [MeSH Descriptor]
Record concept(s)
- anemia, hemolytic, congenital [MeSH concept]
Related MeSH Supplementary Concept(s)
- Rh-Null disease, amorph type [MeSH Supplementary Concept]
- anemia, hereditary spherocytic hemolytic [MeSH Supplementary Concept]
- dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema [MeSH Supplementary Concept]
- heinz body anemias [MeSH Supplementary Concept]
- hemolytic anemia, congenital, with emphysema and cutis laxa [MeSH Supplementary Concept]
- hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities [MeSH Supplementary Concept]
- red cell phospholipid defect with hemolysis [MeSH Supplementary Concept]
- stomatocytosis I [MeSH Supplementary Concept]
- stomatocytosis II [MeSH Supplementary Concept]
- transient erythroblastopenia of childhood [MeSH Supplementary Concept]
- uridine 5-Prime monophosphate hydrolase deficiency, hemolytic anemia due to [MeSH Supplementary Concept]
- xerocytosis, hereditary [MeSH Supplementary Concept]
See also (suggested by CISMeF)
- metabolism, inborn errors [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital haemolytic anaemia [MedDRA LLT]
- Congenital haemolytic anaemia [Bloc CIM-11]
- Congenital haemolytic anaemia NOS [MedDRA LLT]
- Congenital hemolytic anemia [HPO term]
- Congenital hemolytic anemia [MedDRA LLT]
- Congenital hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary Hemolytic Anemia [NCIt concept]
- Hereditary haemolytic anaemia [MedDRA Preferred Term]
- Hereditary haemolytic anaemia NOS [MedDRA LLT]
- Hereditary haemolytic anaemia, unspecified [MedDRA LLT]
- Hereditary haemolytic anaemias [MedDRA LLT]
- Hereditary hemolytic anemia [MedDRA LLT]
- Hereditary hemolytic anemia (disorder) [SNOMED CT concept]
- Hereditary hemolytic anemia, unspecified [ICD-9 code]
- Hereditary hemolytic anemia, unspecified [MedDRA LLT]
- Hereditary hemolytic anemia, unspecified [ICD-10 Sub-category]
- Hereditary hemolytic anemias [MedDRA LLT]
- Hereditary hemolytic anemias [ICD-9 code]
- congenital hemolytic anemia [DO Concept]
- congenital hemolytic anemia [Disease (Nov.)]
- congenital hemolytic anemia, nos [SNOMED Notion]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Hereditary haemolytic anaemia, unspecified [ICD-10 Sub-category (who)]
- Hereditary haemolytic anaemia, unspecified [MedDRA LLT]
- Hereditary hemolytic anemia, unspecified [MedDRA LLT]
- Other hereditary hemolytic anemias [ICD-10 category]
- Other specified hereditary hemolytic anemias [ICD-9 code]
Validated automatic mappings to NTBT
- Other hereditary haemolytic anaemias [ICD-10 category (who)]

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