Hemoglobin C Disease [hemoglobinopatie s hemoglobinem C]

topical
1
Terms

Hemoglobin-C Disease

Persistent link   https://www.medvik.cz/link/D006445
Definition

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.

Annotation
a congen hemolytic anemia; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; do not confuse with HEMOGLOBIN SC DISEASE
DUI
D006445 MeSH Browser
CUI
M0010119
History note
1972(1966)
Public note
1972

C Diseases
C15.378.050 Anemia 1 249
C15.378.050.141 Anemia, Hemolytic 258
C15.378.050.141.150 Anemia, Hemolytic, Congenital 48
C15.378.050.141.150.095 Anemia, Dyserythropoietic, Congenital 16
C15.378.050.141.150.150 Anemia, Sickle Cell 45
C15.378.050.141.150.365 Elliptocytosis, Hereditary 6
C15.378.050.141.150.490 Hemoglobin C Disease 1
C15.378.050.141.150.785 Spherocytosis, Hereditary 43
C15.378.050.141.150.875 Thalassemia 85
C15.378.420 Hemoglobinopathies 68
C15.378.420.155 Anemia, Sickle Cell 45
C15.378.420.463 Hemoglobin C Disease 1
C15.378.420.826 Thalassemia 85
C16.320.070.150 Anemia, Sickle Cell 45
C16.320.070.490 Hemoglobin C Disease 1
C16.320.070.785 Spherocytosis, Hereditary 43
C16.320.070.875 Thalassemia 85
C16.320.365 Hemoglobinopathies 68
C16.320.365.155 Anemia, Sickle Cell 45
C16.320.365.463 Hemoglobin C Disease 1
C16.320.365.826 Thalassemia 85

Hb C disease Disease MeSH Browser