spherocytosis, hereditary

Preferred Label : spherocytosis, hereditary;

MeSH definition : 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.;

MeSH synonym : spherocytoses, hereditary; hereditary spherocytoses;

Wikipedia automatic translation : Hereditary spherocytosis;

MeSH annotation : a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Hereditary spherocytosis;

Details

Origin ID

D013103;

UMLS CUI

C0037889;

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)
- Spherocytic anemia [PASCAL descriptor]
- Spherocytosis [HPO term]
- Spherocytosis [NCIt concept]
- Spherocytosis [MedDRA LLT]
- Spherocytosis (finding) [SNOMED CT concept]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- spherocyte [SNOMED Notion]
Currated CISMeF NLP mapping
- ANAEMIA SPHEROCYTIC [WHO-ART Preferred Term]
- Anaemia spherocytic [MedDRA LLT]
- Anemia spherocytic [MedDRA LLT]
- Hereditary Spherocytosis [NCIt concept]
- Hereditary spherocytosis [ICD-10 Sub-category]
- Hereditary spherocytosis [ICD-11 More detail]
- Hereditary spherocytosis [ICD-9 code]
- Hereditary spherocytosis [ICD-10 Sub-category (who)]
- Hereditary spherocytosis [MedDRA Preferred Term]
- Hereditary spherocytosis [ORDO Disease]
- Hereditary spherocytosis (disorder) [SNOMED CT concept]
- Minkowski-Chauffard syndrome [MedDRA LLT]
- Spherocytic anaemia [MedDRA Preferred Term]
- Spherocytic anemia [MedDRA LLT]
- hereditary spherocytosis [Disease (Nov.)]
- hereditary spherocytosis [DO Concept]
- hereditary spherocytosis, nos [SNOMED Notion]
DO Cross reference
- hereditary spherocytosis [DO Concept]
Indexing information
- band 3, campinas [MeSH Supplementary Concept]
Manual NTBT mappings (CISMeF)
- Rare constitutional hemolytic anemia [ORDO Disease]
- Rare constitutional hemolytic anemia due to a red cell membrane anomaly [ORDO Disease]
ORDO relation(s)
- Hereditary spherocytosis [ORDO Disease]
Record concept(s)
- spherocytosis, hereditary [MeSH concept]
Related MeSH Supplementary Concept(s)
- anemia, hereditary spherocytic hemolytic [MeSH Supplementary Concept]
- goldstein hutt syndrome [MeSH Supplementary Concept]
- spherocytosis, type 1 [MeSH Supplementary Concept]
- spherocytosis, type 3 [MeSH Supplementary Concept]
- spherocytosis, type 4 [MeSH Supplementary Concept]
- spherocytosis, type 5 [MeSH Supplementary Concept]
See also
- anemia, sideroblastic [MeSH Descriptor]
- anion exchange protein 1, erythrocyte [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- ANAEMIA SPHEROCYTIC [WHO-ART Preferred Term]
- Anaemia spherocytic [MedDRA LLT]
- Anemia spherocytic [MedDRA LLT]
- Hereditary Spherocytosis [NCIt concept]
- Hereditary spherocytosis [ORDO Disease]
- Hereditary spherocytosis [ICD-9 code]
- Hereditary spherocytosis [ICD-10 Sub-category]
- Hereditary spherocytosis [ICD-10 Sub-category (who)]
- Hereditary spherocytosis [MedDRA Preferred Term]
- Hereditary spherocytosis [ICD-11 More detail]
- Hereditary spherocytosis (disorder) [SNOMED CT concept]
- Minkowski-Chauffard syndrome [MedDRA LLT]
- Spherocytic anaemia [MedDRA Preferred Term]
- Spherocytic anemia [MedDRA LLT]
- hereditary spherocytosis [DO Concept]
- hereditary spherocytosis [Disease (Nov.)]
- hereditary spherocytosis, nos [SNOMED Notion]

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