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Sickle Cell Trait
MeSH Descriptor Data 2024
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Sickle Cell Trait
Tree Number(s)
C15.378.050.141.150.150.670
C15.378.420.155.668
C16.320.070.150.670
C16.320.365.155.668
Unique ID
D012805
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D012805
Scope Note
The condition of being heterozygous for hemoglobin S.
NLM Classification #
WH 173
Public MeSH Note
91; was see under ANEMIA, SICKLE CELL 1975-90
Online Note
search ANEMIA, SICKLE CELL 1966-74
History Note
91(75); was see under ANEMIA, SICKLE CELL 1975-90
Date Established
1991/01/01
Date of Entry
1999/01/01
Revision Date
2023/02/26
Allowable Qualifiers
blood (BL)
cerebrospinal fluid (CF)
chemically induced (CI)
classification (CL)
complications (CO)
diagnosis (DI)
diagnostic imaging (DG)
diet therapy (DH)
drug therapy (DT)
economics (EC)
embryology (EM)
enzymology (EN)
epidemiology (EP)
ethnology (EH)
etiology (ET)
genetics (GE)
history (HI)
immunology (IM)
metabolism (ME)
microbiology (MI)
mortality (MO)
nursing (NU)
parasitology (PS)
pathology (PA)
physiopathology (PP)
prevention & control (PC)
psychology (PX)
radiotherapy (RT)
rehabilitation (RH)
surgery (SU)
therapy (TH)
urine (UR)
veterinary (VE)
virology (VI)
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Anemia [C15.378.050]
Anemia, Hemolytic [C15.378.050.141]
Anemia, Hemolytic, Congenital [C15.378.050.141.150]
Anemia, Sickle Cell [C15.378.050.141.150.150]
Acute Chest Syndrome [C15.378.050.141.150.150.219]
Hemoglobin SC Disease [C15.378.050.141.150.150.440]
Sickle Cell Trait [C15.378.050.141.150.150.670]
Hemic and Lymphatic Diseases [C15]
Hematologic Diseases [C15.378]
Hemoglobinopathies [C15.378.420]
Anemia, Sickle Cell [C15.378.420.155]
Acute Chest Syndrome [C15.378.420.155.219]
Hemoglobin SC Disease [C15.378.420.155.440]
Sickle Cell Trait [C15.378.420.155.668]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Sickle Cell [C16.320.070.150]
Acute Chest Syndrome [C16.320.070.150.219]
Hemoglobin SC Disease [C16.320.070.150.440]
Sickle Cell Trait [C16.320.070.150.670]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Hemoglobinopathies [C16.320.365]
Anemia, Sickle Cell [C16.320.365.155]
Acute Chest Syndrome [C16.320.365.155.219]
Hemoglobin SC Disease [C16.320.365.155.440]
Sickle Cell Trait [C16.320.365.155.668]
Expand All
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Sickle Cell Trait
Preferred
Concept UI
M0019829
Scope Note
The condition of being heterozygous for hemoglobin S.
Terms
Sickle Cell Trait
Preferred Term
Term UI
T037768
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1975)
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