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Elliptocytosis, Hereditary
MeSH Descriptor Data 2025
Details
Qualifiers
MeSH Tree Structures
Concepts
MeSH Heading
Elliptocytosis, Hereditary
Tree Number(s)
C15.378.050.141.150.365
C16.320.070.365
Unique ID
D004612
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D004612
Annotation
a congen hemolytic anemia; do not use
/congen
& do not coord with
INFANT, NEWBORN, DISEASES
Scope Note
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
Entry Term(s)
Ovalocytosis, Hereditary
See Also
Anemia, Sideroblastic
Public MeSH Note
65
History Note
65(64)
Date Established
1965/01/01
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, Dyserythropoietic, Congenital [C15.378.050.141.150.095]
Anemia, Hemolytic, Congenital Nonspherocytic [C15.378.050.141.150.100]
Anemia, Sickle Cell [C15.378.050.141.150.150]
Elliptocytosis, Hereditary [C15.378.050.141.150.365]
Glucosephosphate Dehydrogenase Deficiency [C15.378.050.141.150.480]
Hemoglobin C Disease [C15.378.050.141.150.490]
Spherocytosis, Hereditary [C15.378.050.141.150.785]
Thalassemia [C15.378.050.141.150.875]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Anemia, Hemolytic, Congenital [C16.320.070]
Anemia, Dyserythropoietic, Congenital [C16.320.070.095]
Anemia, Hemolytic, Congenital Nonspherocytic [C16.320.070.100]
Anemia, Sickle Cell [C16.320.070.150]
Elliptocytosis, Hereditary [C16.320.070.365]
Glucosephosphate Dehydrogenase Deficiency [C16.320.070.480]
Hemoglobin C Disease [C16.320.070.490]
Spherocytosis, Hereditary [C16.320.070.785]
Thalassemia [C16.320.070.875]
Expand All
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Elliptocytosis, Hereditary
Preferred
Concept UI
M0007240
Scope Note
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
Terms
Elliptocytosis, Hereditary
Preferred Term
Term UI
T014076
Date
01/01/1999
LexicalTag
NON
ThesaurusID
NLM (1964)
Ovalocytosis, Hereditary
Term UI
T014077
Date
05/20/1981
LexicalTag
NON
ThesaurusID
UNK (19XX)
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