MeSH Browser

MeSH Heading: Hemoglobin C Disease
Tree Number(s): C15.378.050.141.150.490; C15.378.420.463; C16.320.070.490; C16.320.365.463
Unique ID: D006445
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006445
Annotation: a congen hemolytic anemia; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES; do not confuse with HEMOGLOBIN SC DISEASE
Scope Note: A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
Entry Version: HEMOGLOBIN C DIS
Entry Term(s): Hemoglobin-C Disease
Public MeSH Note: 1972
History Note: 1972(1966)
Date Established: 1972/01/01
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)

Hemoglobin C Disease MeSH Descriptor Data 2025